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Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.

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Title: Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.
Authors: Freua F; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil;; fernando.freua@usp.br., Almeida MEC; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Nóbrega PR; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Paiva ARB; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Della-Ripa B; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Cunha P; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Macedo-Souza LI; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Bueno C; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Lynch DS; Department of Neuromuscular Disease, UCL Institute of Neurology, Queen Square, London, UK., Houlden H; Department of Neuromuscular Disease, UCL Institute of Neurology, Queen Square, London, UK., Lucato LT; Department of Radiology, Hospital das Clínicas da Faculdade de Medicina da Universidade de Sáo Paulo, Sáo Paulo, Brazil;, Kok F; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de Sáo Paulo, Sáo Paulo, Brazil.
Source: Cold Spring Harbor molecular case studies [Cold Spring Harb Mol Case Stud] 2022 Sep 30. Date of Electronic Publication: 2022 Sep 30.
Publication Type: Journal Article
Journal Info: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 101660017 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2373-2873 (Electronic) Linking ISSN: 23732873 NLM ISO Abbreviation: Cold Spring Harb Mol Case Stud Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.
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  Data: <searchLink fieldCode="AU" term="%22Freua+F%22">Freua F</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil;; fernando.freua@usp.br.<br /><searchLink fieldCode="AU" term="%22Almeida+MEC%22">Almeida MEC</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Nóbrega+PR%22">Nóbrega PR</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Paiva+ARB%22">Paiva ARB</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Della-Ripa+B%22">Della-Ripa B</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Cunha+P%22">Cunha P</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Macedo-Souza+LI%22">Macedo-Souza LI</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Bueno+C%22">Bueno C</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Lynch+DS%22">Lynch DS</searchLink>; Department of Neuromuscular Disease, UCL Institute of Neurology, Queen Square, London, UK.<br /><searchLink fieldCode="AU" term="%22Houlden+H%22">Houlden H</searchLink>; Department of Neuromuscular Disease, UCL Institute of Neurology, Queen Square, London, UK.<br /><searchLink fieldCode="AU" term="%22Lucato+LT%22">Lucato LT</searchLink>; Department of Radiology, Hospital das Clínicas da Faculdade de Medicina da Universidade de Sáo Paulo, Sáo Paulo, Brazil;<br /><searchLink fieldCode="AU" term="%22Kok+F%22">Kok F</searchLink>; Neurogenetics Outpatient, Department of Neurology, Hospital das Clínicas da Faculdade de Medicina da Universidade de Sáo Paulo, Sáo Paulo, Brazil.
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  Data: <searchLink fieldCode="JN" term="%22101660017%22">Cold Spring Harbor molecular case studies</searchLink> [Cold Spring Harb Mol Case Stud] 2022 Sep 30. <i>Date of Electronic Publication: </i>2022 Sep 30.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Cold+Spring+Harbor+Laboratory+Press%22">Cold Spring Harbor Laboratory Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101660017 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2373-2873 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223732873%22">23732873 </searchLink><i>NLM ISO Abbreviation: </i>Cold Spring Harb Mol Case Stud <i>Subsets: </i>MEDLINE
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        Value: 10.1101/mcs.a006232
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        Text: English
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      – TitleFull: Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.
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          Dates:
            – D: 30
              M: 09
              Text: 2022 Sep 30
              Type: published
              Y: 2022
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