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1 . Academic Journal
Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporter
저자
by
Menezes, Manoj P.
;
Farrar, Michelle A.
;
Webster, Richard
;
Antony, Jayne
;
O’Brien, Katherine
, et al.
소스
In
Clinical Neurophysiology
January 2016 127(1):911-918
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7 . Academic Journal
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy
저자
by
McMichael, Gai
;
Haan, Eric
;
Gardner, Alison
;
Yap, Tzu Ying
;
Thompson, Suzanna
, et al.
소스
In
European Journal of Medical Genetics
September 2013 56(9):506-509
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7 . Academic Journal
Hereditary peripheral neuropathies of childhood: An overview for clinicians
저자
by
Wilmshurst, Jo M.
;
Ouvrier, Robert
.
소스
In
Neuromuscular Disorders
2011 21(11):763-775
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4 . Academic Journal
Anomalies ultrastructurales des mitochondries axonales chez des patients atteints de formes précoces de maladie de Charcot-Marie-Tooth dues à des mutations de la mitofusine 2
저자
by
Funalot, Benoît
;
Magdelaine, Corinne
;
Sturtz, Franck
;
Ouvrier, Robert
;
Vallat, Jean-Michel
.
소스
In
Bulletin de l'Académie Nationale de Médecine
January 2009 193(1):151-161
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7 . Academic Journal
Magnetic resonance imaging in enterovirus-71, myelin oligodendrocyte glycoprotein antibody, aquaporin-4 antibody, and multiple sclerosis-associated myelitis in children.
저자
by
Tantsis, Esther M
;
Prelog, Kristina
;
Alper, Gulay
;
Benson, Leslie
;
Gorman, Mark
, et al.
소스
Developmental Medicine & Child Neurology
. Sep2019, Vol. 61 Issue 9, p1108-1116. 9p.
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7 . Academic Journal
Feasibility of foot and ankle strength training in childhood Charcot-Marie-Tooth disease
저자
by
Burns, Joshua
;
Raymond, Jacqueline
;
Ouvrier, Robert
.
소스
In
Neuromuscular Disorders
2009 19(12):818-821
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5 . Academic Journal
Natural history of Charcot‐Marie‐Tooth disease during childhood
저자
by
Cornett, Kayla M.D.
;
Menezes, Manoj P.
;
Shy, Rosemary R.
;
Moroni, Isabella
;
Pagliano, Emanuela
, et al.
소스
Annals of Neurology
. Sep 01, 2017 82(3):353-359
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7 . Academic Journal
Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region.
저자
by
Vallat, Jean-Michel
;
Nizon, Mathilde
;
Magee, Alex
;
Isidor, Bertrand
;
Magy, Laurent
, et al.
소스
Journal of Neuropathology & Experimental Neurology; Dec2016, Vol. 75 Issue 12, p1155-1159, 5p
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7 . Academic Journal
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease.
저자
by
Menezes, Manoj P.
;
Rahman, Shamima
;
Bhattacharya, Kaustuv
;
Clark, Damian
;
Christodoulou, John
, et al.
소스
Mitochondrion
. Sep2016, Vol. 30, p162-167. 6p.
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7 . Academic Journal
Auditory neuropathy in Brown-Vialetto-Van Laere syndrome due to riboflavin transporter RFVT2 deficiency.
저자
by
Menezes, Manoj P
;
O'Brien, Katherine
;
Hill, Mandy
;
Webster, Richard
;
Antony, Jayne
, et al.
소스
Developmental Medicine & Child Neurology
. Aug2016, Vol. 58 Issue 8, p848-854. 7p.
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