Jiong Qin


Ontology type: schema:Person     


Person Info

NAME

Jiong

SURNAME

Qin

Publications in SciGraph latest 50 shown

  • 2018-12 TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study in ORPHANET JOURNAL OF RARE DISEASES
  • 2018-06 Busulfan, Fludarabine, and Cyclophosphamide (BFC) conditioning allowed stable engraftment after haplo-identical allogeneic stem cell transplantation in children with adrenoleukodystrophy and mucopolysaccharidosis in BONE MARROW TRANSPLANTATION
  • 2018-06 Oxcarbazepine oral suspension in young pediatric patients with partial seizures and/or generalized tonic–clonic seizures in routine clinical practice in China: a prospective observational study in WORLD JOURNAL OF PEDIATRICS
  • 2018-02 Recombinant Human Erythropoietin Protects Against Hippocampal Damage in Developing Rats with Seizures by Modulating Autophagy via the S6 Protein in a Time-Dependent Manner in NEUROCHEMICAL RESEARCH
  • 2017-12 TuberOus SClerosis registry to increase disease Awareness (TOSCA) – baseline data on 2093 patients in ORPHANET JOURNAL OF RARE DISEASES
  • 2017-12 Oxcarbazepine oral suspension in pediatric patients with partial seizures and/or generalized tonic-clonic seizures: a multi-center, single arm, observational study in China in WORLD JOURNAL OF PEDIATRICS
  • 2012-11 Population pharmacokinetics of lamotrigine in Chinese children with epilepsy in ACTA PHARMACOLOGICA SINICA
  • 2012-02 Niemann-Pick disease type C: analysis of 7 patients in WORLD JOURNAL OF PEDIATRICS
  • 2010-12 Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation in BMC MEDICAL GENETICS
  • 2010-07 Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome in JOURNAL OF HUMAN GENETICS
  • 2009-02 Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease in JOURNAL OF HUMAN GENETICS
  • 2008-08 SCN1A, SCN1B , and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus in JOURNAL OF HUMAN GENETICS
  • 2007-04 Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2006-02 Hydrogen Sulfide and Carbon Monoxide Are in Synergy with Each Other in the Pathogenesis of Recurrent Febrile Seizures in CELLULAR AND MOLECULAR NEUROBIOLOGY
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