Suchergebnisse - "François, P"

PubPharm (148)

1

Intracranial primary synovial sarcoma mimicking a spontaneous cerebral hematoma-a case report and review of the literature

enthalten in: Neuro-Chirurgie | 2022

von Aggad, M. | Gkasdaris, G. | Rousselot, C. | +4

2

Genomic and Phenotypic Characterization of Clostridium botulinum Isolates from an Infant Botulism Case Suggests Adaptation Signatures to the Gut

enthalten in: mBio | 2022

von Douillard, F. | Derman, Y. | Woudstra, C. | +7

3

Radium-223 as an Additional Therapeutic Strategy in Highly Selected Patients With Metastatic Breast Cancer : A Case Report

enthalten in: Frontiers in oncology | 2022

von Houssiau, H. | Duhoux, F. | François, D. | +1

4

BRCA1 Mutation : An Insidious Enemy with Multiple Facets…

enthalten in: Case reports in oncology | 2022

von Godin, P. | Duhoux, F. | Mazzeo, F. | +12

5

Early Death of 2 Siblings Related to Mutations in LMOD2, a Recently Discovered Cause of Neonatal Dilated Cardiomyopathy

enthalten in: CJC open | 2021

von Greenway, S. | Fruitman, D. | Ferrier, R. | +4

6

PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes

enthalten in: Life science alliance | 2019

von Zhao, T. | Goedhart, C. | Sam, P. | +12

7

Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis

enthalten in: European journal of human genetics : EJHG | 2018

von van Dijk, T. | Ferdinandusse, S. | Ruiter, J. | +10

8

Is PNPT1-related hearing loss ever non-syndromic? Whole exome sequencing of adult siblings expands the natural history of PNPT1-related disorders

enthalten in: American journal of medical genetics. Part A | 2018

von Eaton, A. | Bernier, F. | Goedhart, C. | +6

9

Clonal or not clonal? Investigating hospital outbreaks of KPC-producing Klebsiella pneumoniae with whole-genome sequencing

enthalten in: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases | 2017

von Ruppé, E. | Olearo, F. | Pires, D. | +8

10

Mosaic trisomy 1q : a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype

enthalten in: Prenatal diagnosis | 2017

von Bone, K. | Chernos, J. | Perrier, R. | +4

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