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PubPharm (370)
1
Optimization of vigabatrin dosage in children with epileptic spasms : A population pharmacokinetic approach
enthalten in:
British journal of clinical pharmacology
| 2024
von
Molimard, A.
|
Foissac, F.
|
Bouazza, N.
| +9
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2
Neurologic Outcomes and Quality of Life in Children After Extracorporeal Membrane Oxygenation
enthalten in:
Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
| 2024
von
Michel, A.
|
Vedrenne-Cloquet, M.
|
Kossorotoff, M.
| +12
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3
Vitamin deficiencies in children : Lessons from clinical and neuroimaging findings
enthalten in:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
| 2024
von
Dupuy, G.
|
Roux, C.
|
Barrois, R.
| +15
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4
Effect of nusinersen after 3 years of treatment in 57 young children with SMA in terms of SMN2 copy number or type
enthalten in:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
| 2024
von
Audic, F.
|
Dubois, S.
|
Durigneux, J.
| +24
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5
Identifying interindividual variability of social perception and associated brain anatomical correlations in children with autism spectrum disorder using eye-tracking and diffusion tensor imaging MRI (DTI-MRI)
enthalten in:
Cerebral cortex (New York, N.Y. : 1991)
| 2024
von
Vinçon-Leite, A.
|
Saitovitch, A.
|
Lemaître, H.
| +10
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6
Real-World Outcomes in Patients with Spinal Muscular Atrophy Treated with Onasemnogene Abeparvovec Monotherapy : Findings from the RESTORE Registry
enthalten in:
Journal of neuromuscular diseases
| 2024
von
Servais, L.
|
Day, J.
|
De Vivo, D.
| +16
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7
Recurrent "outsider" intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb
enthalten in:
Frontiers in genetics
| 2024
von
Mansour-Hendili, L.
|
Gitiaux, C.
|
Harion, M.
| +16
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8
Combination disease-modifying treatment in spinal muscular atrophy : A proposed classification
enthalten in:
Annals of clinical and translational neurology
| 2023
von
Proud, C.
|
Mercuri, E.
|
Finkel, R.
| +11
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9
An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14
enthalten in:
Neuromuscular disorders : NMD
| 2023
von
Severa, G.
|
Pennisi, A.
|
Barnerias, C.
| +13
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10
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells
enthalten in:
Acta neuropathologica communications
| 2023
von
Cardone, N.
|
Taglietti, V.
|
Baratto, S.
| +14
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Orphanet journal of rare diseases
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Nature genetics
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Developmental medicine and child neurology
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European journal of human genetics : EJHG
9
Brain : a journal of neurology
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Human mutation
9
Journal of inherited metabolic disease
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Developmental medicine & child neurology
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Journal of clinical immunology
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American journal of human genetics
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European journal of medical genetics
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Nerve Tissue Proteins
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STRIDE Registry
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Aicardi-Goutières syndrome
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