View in EDS PDF Full Text

Lessons learned from 40 novel PIGA patients and a review of the literature.

Saved in:
Bibliographic Details
Title: Lessons learned from 40 novel PIGA patients and a review of the literature.
Authors: Bayat A; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark., Knaus A; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-University Bonn, Bonn, Germany., Pendziwiat M; Department of Neuropediatrics, University Medical Center Schleswig-Holstein Christian Albrechts University, Kiel, Germany., Afenjar A; CRMR Congenital Malformations and Diseases of the Cerebellum and Rare Causes of Intellectual Disabilities, Department of Genetics, Sorbonne University, AP-HP, Trousseau Hospital, Paris, France., Barakat TS; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands., Bosch F; Children's Hospital, Fürth, Germany., Callewaert B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium., Calvas P; UMR1056 INSERM-Université de Toulouse, Department of Genetics, University Hospital of Toulouse, Toulouse, France., Ceulemans B; Department of Pediatric Neurology, University Hospital and University of Antwerp, Antwerp, Belgium., Chassaing N; UMR1056 INSERM-Université de Toulouse, Department of Genetics, University Hospital of Toulouse, Toulouse, France., Depienne C; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.; UMR S1127, Inserm U1127, CNRS UMR 7225, Institute of brain and spinal cord, Sorbonne University, Paris, France., Endziniene M; Neurology Department, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania., Ferreira CR; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Moura de Souza CF; Medical Genetics Service, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil., Freihuber C; Department of Pediatric Neurology, AP-HP, GHUEP, Armand Trousseau University Hospital, Paris, France.; GRC ConCer-LD, Sorbonne University, UPMC University of Paris 06, Paris, France., Ganesan S; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Epilepsy NeuroGenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., Gataullina S; Sleep Disorders Center, AP-HP, Antoine-Béclère Hospital, Clamart, France.; Department of Pediatrics and Neonatal Intensive Care, André Grégoire Hospital, Montreuil, France., Guerrini R; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Department of Neuroscience, A. Meyer Children's Hospital, University of Florence, Florence, Italy., Guerrot AM; Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, Normandy University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Rouen, France., Hansen L; Department of Cellular and Molecular Medicine, Faculty of Health Science, Copenhagen Center for Glycomics, Copenhagen, Denmark., Jezela-Stanek A; Department of Genetics and Clinical Immunology, National Institute of Tuberculosis and Lung Diseases, Warsaw, Poland., Karsenty C; Neuropediatrics Department, University Hospital of Toulouse, Toulouse, France., Kievit A; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands., Kooy FR; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Korff CM; Pediatric Neurology Unit, Department of the Woman, Child, and Adolescent, University Hospitals Geneva, Geneva, Switzerland., Kragh Hansen J; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark., Larsen M; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark., Layet V; Department of Genetics, Du Havre Hospital, Le Havre, France., Lesca G; Department of Medical Genetics, Lyon University Hospital, Lyon, France.; Institut Neuromyogene, University Claude Bernard Lyon 1, Lyon University, Lyon, France., McBride KL; Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.; Center for Cardiovascular Research, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, Ohio State University, Columbus, Ohio, USA., Meuwissen M; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium., Mignot C; APHP, Department of Genetics, Pitié-Salpêtrière Hospital, Reference Center for Rare Causes of Intellectual Disabilities, Paris, France.; Department of Genetics, Inserm U1127, CNRS UMR 7225, Institute for brain and spinal cord, ICM, AP-HP, De la Pitié Salpêtrière Hospital, Sorbonne University, Paris, France., Montomoli M; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Department of Neuroscience, A. Meyer Children's Hospital, University of Florence, Florence, Italy., Moore H; Greenwood Genetic Center, Greenwood, South Carolina, USA., Naudion S; Department of Genetics, University of Bordeaux, Bordeaux, France., Nava C; Department of Genetics, Inserm U1127, CNRS UMR 7225, Institute for brain and spinal cord, ICM, AP-HP, De la Pitié Salpêtrière Hospital, Sorbonne University, Paris, France., Nougues MC; Department of Neuropaediatrics, Armand Trousseau Hospital, APHP, Paris, France., Parrini E; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Department of Neuroscience, A. Meyer Children's Hospital, University of Florence, Florence, Italy., Pastore M; Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, Ohio State University, Columbus, Ohio, USA., Schelhaas JH; Department of Epilepsy, Zwolle, the Netherlands., Skinner S; Greenwood Genetic Center, Greenwood, South Carolina, USA., Szczałuba K; Department of Medical Genetics, Warsaw Medical University, Warsaw, Poland., Thomas A; Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA., Thomassen M; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark., Tranebjaerg L; Department of Clinical Genetics, Rigshospitalet/Kennedy Center, Glostrup, Denmark.; Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark., van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands., Wolfe LA; Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, Maryland, USA.; Section of Human Biochemical Genetics, National Human Genome Research Institute, Bethesda, Maryland, USA., Lal D; Cologne Center for Genomics, University Hospital Cologne, University of Cologne, Cologne, Germany.; Stanley Center for Psychiatric Research, Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts, USA.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.; Genomic Medicine Institute, Lerner Research Institute Cleveland Clinic, Cleveland, Ohio, USA., Gardella E; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Department of Clinical Neurophysiology, Danish Epilepsy Center, Dianalund, Denmark., Bomme Ousager L; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark., Brünger T; Cologne Center for Genomics, University Hospital Cologne, University of Cologne, Cologne, Germany., Helbig I; Department of Neuropediatrics, University Medical Center Schleswig-Holstein Christian Albrechts University, Kiel, Germany.; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Epilepsy NeuroGenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Neurology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, USA., Krawitz P; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-University Bonn, Bonn, Germany., Møller RS; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.
Source: Epilepsia [Epilepsia] 2020 Jun; Vol. 61 (6), pp. 1142-1155. Date of Electronic Publication: 2020 May 26.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
Journal Info: Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 32452540
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Lessons learned from 40 novel PIGA patients and a review of the literature.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Bayat+A%22">Bayat A</searchLink>; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.<br /><searchLink fieldCode="AU" term="%22Knaus+A%22">Knaus A</searchLink>; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-University Bonn, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Pendziwiat+M%22">Pendziwiat M</searchLink>; Department of Neuropediatrics, University Medical Center Schleswig-Holstein Christian Albrechts University, Kiel, Germany.<br /><searchLink fieldCode="AU" term="%22Afenjar+A%22">Afenjar A</searchLink>; CRMR Congenital Malformations and Diseases of the Cerebellum and Rare Causes of Intellectual Disabilities, Department of Genetics, Sorbonne University, AP-HP, Trousseau Hospital, Paris, France.<br /><searchLink fieldCode="AU" term="%22Barakat+TS%22">Barakat TS</searchLink>; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Bosch+F%22">Bosch F</searchLink>; Children's Hospital, Fürth, Germany.<br /><searchLink fieldCode="AU" term="%22Callewaert+B%22">Callewaert B</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Calvas+P%22">Calvas P</searchLink>; UMR1056 INSERM-Université de Toulouse, Department of Genetics, University Hospital of Toulouse, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Ceulemans+B%22">Ceulemans B</searchLink>; Department of Pediatric Neurology, University Hospital and University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Chassaing+N%22">Chassaing N</searchLink>; UMR1056 INSERM-Université de Toulouse, Department of Genetics, University Hospital of Toulouse, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Depienne+C%22">Depienne C</searchLink>; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.; UMR S1127, Inserm U1127, CNRS UMR 7225, Institute of brain and spinal cord, Sorbonne University, Paris, France.<br /><searchLink fieldCode="AU" term="%22Endziniene+M%22">Endziniene M</searchLink>; Neurology Department, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.<br /><searchLink fieldCode="AU" term="%22Ferreira+CR%22">Ferreira CR</searchLink>; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Moura+de+Souza+CF%22">Moura de Souza CF</searchLink>; Medical Genetics Service, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.<br /><searchLink fieldCode="AU" term="%22Freihuber+C%22">Freihuber C</searchLink>; Department of Pediatric Neurology, AP-HP, GHUEP, Armand Trousseau University Hospital, Paris, France.; GRC ConCer-LD, Sorbonne University, UPMC University of Paris 06, Paris, France.<br /><searchLink fieldCode="AU" term="%22Ganesan+S%22">Ganesan S</searchLink>; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Epilepsy NeuroGenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Gataullina+S%22">Gataullina S</searchLink>; Sleep Disorders Center, AP-HP, Antoine-Béclère Hospital, Clamart, France.; Department of Pediatrics and Neonatal Intensive Care, André Grégoire Hospital, Montreuil, France.<br /><searchLink fieldCode="AU" term="%22Guerrini+R%22">Guerrini R</searchLink>; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Department of Neuroscience, A. Meyer Children's Hospital, University of Florence, Florence, Italy.<br /><searchLink fieldCode="AU" term="%22Guerrot+AM%22">Guerrot AM</searchLink>; Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, Normandy University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Hansen+L%22">Hansen L</searchLink>; Department of Cellular and Molecular Medicine, Faculty of Health Science, Copenhagen Center for Glycomics, Copenhagen, Denmark.<br /><searchLink fieldCode="AU" term="%22Jezela-Stanek+A%22">Jezela-Stanek A</searchLink>; Department of Genetics and Clinical Immunology, National Institute of Tuberculosis and Lung Diseases, Warsaw, Poland.<br /><searchLink fieldCode="AU" term="%22Karsenty+C%22">Karsenty C</searchLink>; Neuropediatrics Department, University Hospital of Toulouse, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Kievit+A%22">Kievit A</searchLink>; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Kooy+FR%22">Kooy FR</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Korff+CM%22">Korff CM</searchLink>; Pediatric Neurology Unit, Department of the Woman, Child, and Adolescent, University Hospitals Geneva, Geneva, Switzerland.<br /><searchLink fieldCode="AU" term="%22Kragh+Hansen+J%22">Kragh Hansen J</searchLink>; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.<br /><searchLink fieldCode="AU" term="%22Larsen+M%22">Larsen M</searchLink>; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.<br /><searchLink fieldCode="AU" term="%22Layet+V%22">Layet V</searchLink>; Department of Genetics, Du Havre Hospital, Le Havre, France.<br /><searchLink fieldCode="AU" term="%22Lesca+G%22">Lesca G</searchLink>; Department of Medical Genetics, Lyon University Hospital, Lyon, France.; Institut Neuromyogene, University Claude Bernard Lyon 1, Lyon University, Lyon, France.<br /><searchLink fieldCode="AU" term="%22McBride+KL%22">McBride KL</searchLink>; Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.; Center for Cardiovascular Research, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, Ohio State University, Columbus, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Meuwissen+M%22">Meuwissen M</searchLink>; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Mignot+C%22">Mignot C</searchLink>; APHP, Department of Genetics, Pitié-Salpêtrière Hospital, Reference Center for Rare Causes of Intellectual Disabilities, Paris, France.; Department of Genetics, Inserm U1127, CNRS UMR 7225, Institute for brain and spinal cord, ICM, AP-HP, De la Pitié Salpêtrière Hospital, Sorbonne University, Paris, France.<br /><searchLink fieldCode="AU" term="%22Montomoli+M%22">Montomoli M</searchLink>; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Department of Neuroscience, A. Meyer Children's Hospital, University of Florence, Florence, Italy.<br /><searchLink fieldCode="AU" term="%22Moore+H%22">Moore H</searchLink>; Greenwood Genetic Center, Greenwood, South Carolina, USA.<br /><searchLink fieldCode="AU" term="%22Naudion+S%22">Naudion S</searchLink>; Department of Genetics, University of Bordeaux, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Nava+C%22">Nava C</searchLink>; Department of Genetics, Inserm U1127, CNRS UMR 7225, Institute for brain and spinal cord, ICM, AP-HP, De la Pitié Salpêtrière Hospital, Sorbonne University, Paris, France.<br /><searchLink fieldCode="AU" term="%22Nougues+MC%22">Nougues MC</searchLink>; Department of Neuropaediatrics, Armand Trousseau Hospital, APHP, Paris, France.<br /><searchLink fieldCode="AU" term="%22Parrini+E%22">Parrini E</searchLink>; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Department of Neuroscience, A. Meyer Children's Hospital, University of Florence, Florence, Italy.<br /><searchLink fieldCode="AU" term="%22Pastore+M%22">Pastore M</searchLink>; Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, Ohio State University, Columbus, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Schelhaas+JH%22">Schelhaas JH</searchLink>; Department of Epilepsy, Zwolle, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Skinner+S%22">Skinner S</searchLink>; Greenwood Genetic Center, Greenwood, South Carolina, USA.<br /><searchLink fieldCode="AU" term="%22Szczałuba+K%22">Szczałuba K</searchLink>; Department of Medical Genetics, Warsaw Medical University, Warsaw, Poland.<br /><searchLink fieldCode="AU" term="%22Thomas+A%22">Thomas A</searchLink>; Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.<br /><searchLink fieldCode="AU" term="%22Thomassen+M%22">Thomassen M</searchLink>; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.<br /><searchLink fieldCode="AU" term="%22Tranebjaerg+L%22">Tranebjaerg L</searchLink>; Department of Clinical Genetics, Rigshospitalet/Kennedy Center, Glostrup, Denmark.; Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.<br /><searchLink fieldCode="AU" term="%22van+Slegtenhorst+M%22">van Slegtenhorst M</searchLink>; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Wolfe+LA%22">Wolfe LA</searchLink>; Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, Maryland, USA.; Section of Human Biochemical Genetics, National Human Genome Research Institute, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Lal+D%22">Lal D</searchLink>; Cologne Center for Genomics, University Hospital Cologne, University of Cologne, Cologne, Germany.; Stanley Center for Psychiatric Research, Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts, USA.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.; Genomic Medicine Institute, Lerner Research Institute Cleveland Clinic, Cleveland, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Gardella+E%22">Gardella E</searchLink>; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Department of Clinical Neurophysiology, Danish Epilepsy Center, Dianalund, Denmark.<br /><searchLink fieldCode="AU" term="%22Bomme+Ousager+L%22">Bomme Ousager L</searchLink>; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.<br /><searchLink fieldCode="AU" term="%22Brünger+T%22">Brünger T</searchLink>; Cologne Center for Genomics, University Hospital Cologne, University of Cologne, Cologne, Germany.<br /><searchLink fieldCode="AU" term="%22Helbig+I%22">Helbig I</searchLink>; Department of Neuropediatrics, University Medical Center Schleswig-Holstein Christian Albrechts University, Kiel, Germany.; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Epilepsy NeuroGenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Neurology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Krawitz+P%22">Krawitz P</searchLink>; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-University Bonn, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Møller+RS%22">Møller RS</searchLink>; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%222983306R%22">Epilepsia</searchLink> [Epilepsia] 2020 Jun; Vol. 61 (6), pp. 1142-1155. <i>Date of Electronic Publication: </i>2020 May 26.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, Non-U.S. Gov't; Review
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Blackwell+Science%22">Blackwell Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>2983306R <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1528-1167 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200139580%22">00139580 </searchLink><i>NLM ISO Abbreviation: </i>Epilepsia <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32452540
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1111/epi.16545
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1142
    Titles:
      – TitleFull: Lessons learned from 40 novel PIGA patients and a review of the literature.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Bayat A
      – PersonEntity:
          Name:
            NameFull: Knaus A
      – PersonEntity:
          Name:
            NameFull: Pendziwiat M
      – PersonEntity:
          Name:
            NameFull: Afenjar A
      – PersonEntity:
          Name:
            NameFull: Barakat TS
      – PersonEntity:
          Name:
            NameFull: Bosch F
      – PersonEntity:
          Name:
            NameFull: Callewaert B
      – PersonEntity:
          Name:
            NameFull: Calvas P
      – PersonEntity:
          Name:
            NameFull: Ceulemans B
      – PersonEntity:
          Name:
            NameFull: Chassaing N
      – PersonEntity:
          Name:
            NameFull: Depienne C
      – PersonEntity:
          Name:
            NameFull: Endziniene M
      – PersonEntity:
          Name:
            NameFull: Ferreira CR
      – PersonEntity:
          Name:
            NameFull: Moura de Souza CF
      – PersonEntity:
          Name:
            NameFull: Freihuber C
      – PersonEntity:
          Name:
            NameFull: Ganesan S
      – PersonEntity:
          Name:
            NameFull: Gataullina S
      – PersonEntity:
          Name:
            NameFull: Guerrini R
      – PersonEntity:
          Name:
            NameFull: Guerrot AM
      – PersonEntity:
          Name:
            NameFull: Hansen L
      – PersonEntity:
          Name:
            NameFull: Jezela-Stanek A
      – PersonEntity:
          Name:
            NameFull: Karsenty C
      – PersonEntity:
          Name:
            NameFull: Kievit A
      – PersonEntity:
          Name:
            NameFull: Kooy FR
      – PersonEntity:
          Name:
            NameFull: Korff CM
      – PersonEntity:
          Name:
            NameFull: Kragh Hansen J
      – PersonEntity:
          Name:
            NameFull: Larsen M
      – PersonEntity:
          Name:
            NameFull: Layet V
      – PersonEntity:
          Name:
            NameFull: Lesca G
      – PersonEntity:
          Name:
            NameFull: McBride KL
      – PersonEntity:
          Name:
            NameFull: Meuwissen M
      – PersonEntity:
          Name:
            NameFull: Mignot C
      – PersonEntity:
          Name:
            NameFull: Montomoli M
      – PersonEntity:
          Name:
            NameFull: Moore H
      – PersonEntity:
          Name:
            NameFull: Naudion S
      – PersonEntity:
          Name:
            NameFull: Nava C
      – PersonEntity:
          Name:
            NameFull: Nougues MC
      – PersonEntity:
          Name:
            NameFull: Parrini E
      – PersonEntity:
          Name:
            NameFull: Pastore M
      – PersonEntity:
          Name:
            NameFull: Schelhaas JH
      – PersonEntity:
          Name:
            NameFull: Skinner S
      – PersonEntity:
          Name:
            NameFull: Szczałuba K
      – PersonEntity:
          Name:
            NameFull: Thomas A
      – PersonEntity:
          Name:
            NameFull: Thomassen M
      – PersonEntity:
          Name:
            NameFull: Tranebjaerg L
      – PersonEntity:
          Name:
            NameFull: van Slegtenhorst M
      – PersonEntity:
          Name:
            NameFull: Wolfe LA
      – PersonEntity:
          Name:
            NameFull: Lal D
      – PersonEntity:
          Name:
            NameFull: Gardella E
      – PersonEntity:
          Name:
            NameFull: Bomme Ousager L
      – PersonEntity:
          Name:
            NameFull: Brünger T
      – PersonEntity:
          Name:
            NameFull: Helbig I
      – PersonEntity:
          Name:
            NameFull: Krawitz P
      – PersonEntity:
          Name:
            NameFull: Møller RS
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 06
              Text: 2020 Jun
              Type: published
              Y: 2020
          Identifiers:
            – Type: issn-electronic
              Value: 1528-1167
          Numbering:
            – Type: volume
              Value: 61
            – Type: issue
              Value: 6
          Titles:
            – TitleFull: Epilepsia
              Type: main
ResultId 1