Suchergebnisse - "Rivier, F"

PubPharm (140)

1

Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype

enthalten in: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology | 2022

von Coste, T. | Aloui, C. | Petit, F. | +8

2

Prognostic value of contrast-enhanced MRI in Guillain-Barré syndrome in children

enthalten in: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 2022

von Althubaiti, F. | Guiomard, C. | Rivier, F. | +2

3

Rare metabolic disease mimicking COL4A1/ COL4A2 fetal brain phenotype

enthalten in: Ultrasound in Obstetrics & Gynecology | 2022

von Coste, T. | Aloui, C. | Petit, F. | +8

4

Clinical Phenotype in an Early-Onset French Pediatric Population : Charcot-Marie-Tooth's Disease Type 2A

enthalten in: Neuropediatrics | 2021

von Majorel-Beraud, C. | Baudou, E. | Walther-Louvier, U. | +5

5

Arthrogryposis in children : Etiological assessments and preparation of a protocol for etiological investigations

enthalten in: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 2018

von Wallach, E. | Walther-Louvier, U. | Espil-Taris, C. | +3

6

Corrigendum to "22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd-7th October 2017" [Neuromuscular Disorders 27S2 (2017) S51-S270

enthalten in: Neuromuscular disorders : NMD | 2017

von Rendu, J. | Bosson, C. | Roux-Buisson, N. | +9

7

Bilateral facial nerve palsy associated with Epstein-Barr virus infection in a 3-year-old boy

enthalten in: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 2017

von Grassin, M. | Rolland, A. | Leboucq, N. | +3

8

Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series

enthalten in: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 2016

von Raignoux, J. | Walther-Louvier, U. | Espil, C. | +4

9

Maladies neuromusculaires congénitales à expression respiratoire néonatale à l’exclusion de la dystrophie myotonique de type 1 et de l’amyotrophie spinale infantile. Stratégie d’exploration d’après une série de 19 enfants

enthalten in: Archives de pédiatrie | 2016

von Raignoux, J. | Walther-Louvier, U. | Espil, C. | +4

10

Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series

enthalten in: Archives de pédiatrie | 2016

von Raignoux, J. | Walther-Louvier, U. | Espil, C. | +4

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