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Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.
Dehnavi, Ali Zare; Bemanalizadeh, Maryam; Kahani, Seyyed Mohammad; Ashrafi, Mahmoud Reza; Rohani, Mohammad; Toosi, Mehran Beiraghi; Heidari, Morteza; Hosseinpour, Sareh; Amini, Behnam; Zokaei, Shaghayegh; Rezaei, Zahra; Aryan, Hajar; Amanat, Man; Vahidnezhad, Hassan; Mohammadi, Pouria; Garshasbi, Masoud; Tavasoli, Ali Reza.
Affiliation
  • Dehnavi AZ; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Bemanalizadeh M; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Kahani SM; Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Ashrafi MR; Faculty of Medical Sciences, Department of Medical Genetics, Tarbiat Modares University, Tehran, Iran.
  • Rohani M; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Toosi MB; Skull Base Research Center, The Five Senses Health Institute, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Heidari M; Department of Neurology, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Hosseinpour S; Department of Pediatrics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Amini B; Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Zokaei S; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Rezaei Z; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Aryan H; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Amanat M; Dr. Farhud's Genetic Clinic, Tehran, Iran.
  • Vahidnezhad H; School of Advanced Medical Science, Islamic Azad University, Tehran, Iran.
  • Mohammadi P; Department of Pediatrics, Division of Pediatric Neurology, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Garshasbi M; Dr. Farhud's Genetic Clinic, Tehran, Iran.
  • Tavasoli AR; National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.
Orphanet J Rare Dis ; 18(1): 177, 2023 07 05.
Article in En | MEDLINE | ID: mdl-37403138
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neuroaxonal Dystrophies / Parkinsonian Disorders Type of study: Guideline / Prognostic_studies / Risk_factors_studies Limits: Adult / Child / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2023 Document type: Article Affiliation country: Irán Country of publication: Reino Unido
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neuroaxonal Dystrophies / Parkinsonian Disorders Type of study: Guideline / Prognostic_studies / Risk_factors_studies Limits: Adult / Child / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2023 Document type: Article Affiliation country: Irán Country of publication: Reino Unido