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Cerebral creatine deficiency disorders - A clinical, genetic and follow up study from India.
Passi, Gouri Rao; Pandey, Swati; Devi, Akella Radha Rama; Konanki, Ramesh; Jain, Abhishek Ravindra; Bhatnagar, Shweta; Tripathi, Ruchi; Jain, Vivek.
Affiliation
  • Passi GR; Department of Pediatrics & Pediatric Neurology, Choithram Hospital & Research Centre, Indore, India.
  • Pandey S; Department of Pediatrics & Pediatric Neurology, Santokba Durlabhji Memorial Hospital, Jaipur, India.
  • Devi ARR; Department of Genetics and Pediatric Neurology, Rainbow Children's Hospital, Hyderabad, India.
  • Konanki R; Department of Genetics and Pediatric Neurology, Rainbow Children's Hospital, Hyderabad, India.
  • Jain AR; Department of Genetics and Pediatric Neurology, Rainbow Children's Hospital, Hyderabad, India.
  • Bhatnagar S; Department of Radio Diagnosis, Sri Aurobindo Institute of Medical Sciences, Indore, India.
  • Tripathi R; Department of Pediatrics & Pediatric Neurology, Choithram Hospital & Research Centre, Indore, India.
  • Jain V; Department of Pediatrics & Pediatric Neurology, Santokba Durlabhji Memorial Hospital, Jaipur, India. Electronic address: vivek.jain@sdmh.in.
Brain Dev ; 44(4): 271-280, 2022 Apr.
Article in En | MEDLINE | ID: mdl-34974949
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Creatine / Brain Diseases, Metabolic, Inborn / Mental Retardation, X-Linked / Guanidinoacetate N-Methyltransferase / Plasma Membrane Neurotransmitter Transport Proteins / Neurodevelopmental Disorders / Language Development Disorders / Movement Disorders Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Brain Dev Year: 2022 Document type: Article Affiliation country: India Country of publication: Países Bajos
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Creatine / Brain Diseases, Metabolic, Inborn / Mental Retardation, X-Linked / Guanidinoacetate N-Methyltransferase / Plasma Membrane Neurotransmitter Transport Proteins / Neurodevelopmental Disorders / Language Development Disorders / Movement Disorders Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Brain Dev Year: 2022 Document type: Article Affiliation country: India Country of publication: Países Bajos