Hôpital Saint-Vincent-de-Paul View Homepage


Ontology type: grid:Healthcare  | foaf:Organization     


Organization Info

Publications in SciGraph latest 20 shown

  • 2019-04 Intra-monocyte Pharmacokinetics of Imiglucerase Supports a Possible Personalized Management of Gaucher Disease Type 1 in CLINICAL PHARMACOKINETICS
  • 2019-03 Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-01 Interleukin-22 protects against non-typeable Haemophilus influenzae infection: alteration during chronic obstructive pulmonary disease in MUCOSAL IMMUNOLOGY
  • 2016-06 A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-12 PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-12 Impact of imiglucerase supply constraint on the therapeutic management and course of disease in French patients with Gaucher disease type 1 in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-07 Presentation and endoscopic management of sigmoid volvulus in children in EUROPEAN JOURNAL OF PEDIATRICS
  • 2014-12 Study of proximal femoral bone perfusion with 3D T1 dynamic contrast-enhanced MRI: a feasibility study in EUROPEAN RADIOLOGY
  • 2014-02 Traitements systémiques de première et de deuxième lignes des patients atteints d’un mélanome cutané métastatique (hors métastase cérébrale) : Recommandations nationales françaises in ONCOLOGIE
  • 2013-06 The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-05 Assessment of reduced field of view in diffusion tensor imaging of the lumbar nerve roots at 3 T in EUROPEAN RADIOLOGY
  • 2013-01 12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-12 The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients in ORPHANET JOURNAL OF RARE DISEASES
  • 2012-04 Anatomic response of occult choroidal neovascularization to intravitreal ranibizumab: a study by indocyanine green angiography in GRAEFE'S ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
  • 2012-01 Interval between onset of symptoms and diagnosis of medulloblastoma in children: distribution and determinants in a population-based study in EUROPEAN JOURNAL OF PEDIATRICS
  • 2011-12 Efficacy of epicutaneous immunotherapy (EPIT) in a new model of peanut-induced eosinophilic esophagitis (EoE) and allergic enterpathy (AE) in CLINICAL AND TRANSLATIONAL ALLERGY
  • 2011-12 Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene in ORPHANET JOURNAL OF RARE DISEASES
  • 2011-11 Validation francophone de la grille d’évaluation de la douleur-déficience intellectuelle – version postopératoire in JOURNAL CANADIEN D'ANESTHÉSIE
  • 2011-09 Traitement endoscopique par « rendez-vous » de l’obstruction complète d’une anastomose iléorectale in ACTA ENDOSCOPICA
  • 2011-06 Identification of new autoantibody specificities directed at proteins involved in the transforming growth factor β pathway in patients with systemic sclerosis in ARTHRITIS RESEARCH & THERAPY
  • JSON-LD is the canonical representation for SciGraph data.

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    Download the RDF metadata as:  json-ld nt turtle xml License info

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    This table displays all metadata directly associated to this object as RDF triples.

    79 TRIPLES      11 PREDICATES      12 URIs      5 LITERALS

    Subject Predicate Object
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