Necker-Enfants Malades Hospital View Homepage


Ontology type: grid:Healthcare  | foaf:Organization     


Organization Info

NAME

Necker-Enfants Malades Hospital

HOMEPAGE

http://hopital-necker.aphp.fr/

ADDRESS

http://www.grid.ac/institutes/grid.412134.1/address-0

Publications in SciGraph latest 20 shown

  • 2019-12 The class 3 PI3K coordinates autophagy and mitochondrial lipid catabolism by controlling nuclear receptor PPARα. in NATURE COMMUNICATIONS
  • 2019-12 Betaine anhydrous in homocystinuria: results from the RoCH registry in ORPHANET JOURNAL OF RARE DISEASES
  • 2019-12 Within-Host Genomic Diversity of Candida albicans in Healthy Carriers in SCIENTIFIC REPORTS
  • 2019-12 Italian translation, cultural adaptation, and pilot testing of a questionnaire to assess family burden in inherited ichthyoses in ITALIAN JOURNAL OF PEDIATRICS
  • 2019-12 Author Correction: 22q13 deletion syndrome: communication disorder or autism? Evidence from a specific clinical and neurophysiological phenotype in TRANSLATIONAL PSYCHIATRY
  • 2019-12 Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly in NATURE COMMUNICATIONS
  • 2019-05 Overgrowth syndromes — clinical and molecular aspects and tumour risk in NATURE REVIEWS ENDOCRINOLOGY
  • 2019-04-03 Author Correction: Targeted therapy in patients with PIK3CA-related overgrowth syndrome in NATURE
  • 2019-04 IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients in GENETICS IN MEDICINE
  • 2019-04 Duplication of 10q24 locus: broadening the clinical and radiological spectrum in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2019-04 A future for CD3 antibodies in immunotherapy of type 1 diabetes in DIABETOLOGIA
  • 2019-04 Intra-monocyte Pharmacokinetics of Imiglucerase Supports a Possible Personalized Management of Gaucher Disease Type 1 in CLINICAL PHARMACOKINETICS
  • 2019-04 Growth impairment and limited range of joint motion in children should raise suspicion of an attenuated form of mucopolysaccharidosis: expert opinion in EUROPEAN JOURNAL OF PEDIATRICS
  • 2019-04 Five-year outcome of children with idiopathic nephrotic syndrome: the NEPHROVIR population-based cohort study in PEDIATRIC NEPHROLOGY
  • 2019-03-29 De novo and biallelic DEAF1 variants cause a phenotypic spectrum in GENETICS IN MEDICINE
  • 2019-03-25 Targeting Type IV pili as an antivirulence strategy against invasive meningococcal disease in NATURE MICROBIOLOGY
  • 2019-03-13 The Impact of Atypical Sensory Processing on Adaptive Functioning and Maladaptive Behaviors in Autism Spectrum Disorder During Childhood: Results From the ELENA Cohort in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2019-03-12 Nephrotic syndrome and mitochondrial disorders: answers in PEDIATRIC NEPHROLOGY
  • 2019-03-12 Nephrotic syndrome and mitochondrial disorders: Questions in PEDIATRIC NEPHROLOGY
  • 2019-03-05 Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction in JOURNAL OF CLINICAL IMMUNOLOGY
  • JSON-LD is the canonical representation for SciGraph data.

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