Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69.
Saved in:
| Title: | Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69. |
|---|---|
| Authors: | Sadr Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Ghasemi A; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran., Rohani M; Department of Neurology, The Five Senses Health Institute, Iran University of Medical Sciences, Tehran, Iran., Khorram Khorshid HR; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Habibi-Kavashkohie MR; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; CHU Sainte Justine Research Center, University of Montreal, Montréal, Canada., Mohammadi Y; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. afaghalavi@gmail.com.; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran. afaghalavi@gmail.com. |
| Source: | Neurogenetics [Neurogenetics] 2024 Nov 28; Vol. 26 (1), pp. 12. Date of Electronic Publication: 2024 Nov 28. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Electronic Cited Medium: Internet ISSN: 1364-6753 (Electronic) Linking ISSN: 13646745 NLM ISO Abbreviation: Neurogenetics Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39607444 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Sadr+Z%22">Sadr Z</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Ghasemi+A%22">Ghasemi A</searchLink>; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Rohani+M%22">Rohani M</searchLink>; Department of Neurology, The Five Senses Health Institute, Iran University of Medical Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Khorram+Khorshid+HR%22">Khorram Khorshid HR</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Habibi-Kavashkohie+MR%22">Habibi-Kavashkohie MR</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; CHU Sainte Justine Research Center, University of Montreal, Montréal, Canada.<br /><searchLink fieldCode="AU" term="%22Mohammadi+Y%22">Mohammadi Y</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Alavi+A%22">Alavi A</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. afaghalavi@gmail.com.; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran. afaghalavi@gmail.com. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229709714%22">Neurogenetics</searchLink> [Neurogenetics] 2024 Nov 28; Vol. 26 (1), pp. 12. <i>Date of Electronic Publication: </i>2024 Nov 28. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer-Verlag%22">Springer-Verlag </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9709714 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1364-6753 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2213646745%22">13646745 </searchLink><i>NLM ISO Abbreviation: </i>Neurogenetics <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39607444 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s10048-024-00789-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 12 Titles: – TitleFull: Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Sadr Z – PersonEntity: Name: NameFull: Ghasemi A – PersonEntity: Name: NameFull: Rohani M – PersonEntity: Name: NameFull: Khorram Khorshid HR – PersonEntity: Name: NameFull: Habibi-Kavashkohie MR – PersonEntity: Name: NameFull: Mohammadi Y – PersonEntity: Name: NameFull: Alavi A IsPartOfRelationships: – BibEntity: Dates: – D: 28 M: 11 Text: 2024 Nov 28 Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1364-6753 Numbering: – Type: volume Value: 26 – Type: issue Value: 1 Titles: – TitleFull: Neurogenetics Type: main |
| ResultId | 1 |