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Manoj P Menezes

Showing results (11-20 of 68) with videos related to

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Neurology|October 17, 2020
Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor NeuropathyHerminia Argente-Escrig, Joshua Burns, Gabrielle Donlevy, et al.
Hip International : the Journal of Clinical and Experimental Research on Hip Pathology and Therapy|June 28, 2021
Reliability and sensitivity of radiographic measures of hip dysplasia in childhood Charcot-Marie-Tooth diseaseLeanne N Dwan, Paul Gibbons, Kamal Jamil, et al.
Journal of Physiotherapy|May 27, 2014
Randomised controlled trial protocol of foot and ankle exercise for children with Charcot-Marie-Tooth diseaseAmy D Sman, Jacqueline Raymond, Kathryn M Refshauge, et al.
Developmental Medicine and Child Neurology|February 27, 2016
Auditory neuropathy in Brown-Vialetto-Van Laere syndrome due to riboflavin transporter RFVT2 deficiencyManoj P Menezes, Katherine O'Brien, Mandy Hill, et al.
Journal of Paediatrics and Child Health|August 24, 2022
Steroid-responsive aseptic meningitis with raised intracranial pressure syndrome associated with myelin oligodendrocyte glycoprotein autoantibodiesWui-Kwan Wong, Christopher Troedson, Ken Peacock, et al.
Journal of the Peripheral Nervous System : JPNS|March 6, 2024
Development of a functional outcome measure for riboflavin transporter deficiencyJack R Fennessy, Gabrielle A Donlevy, Marnee J McKay, et al.
Developmental Medicine and Child Neurology|September 10, 2024
Long-term outcomes in children with riboflavin transporter deficiency and surveillance recommendationsJack R Fennessy, Kayla M D Cornett, Gabrielle A Donlevy, et al.
Neurology|June 10, 2020
Prenusinersen economic and health-related quality of life burden of spinal muscular atrophyGeorgina M Chambers, Stella Nalukwago Settumba, Kate A Carey, et al.
Genes & Diseases|March 22, 2024
<i>C. elegans</i> model of riboflavin transporter deficiency (RTD) disorder reveals deficits in synaptic transmission and movementRamesh K Narayanan, Gonzalo Perez-Siles, Kamila A Marzec, et al.
Neuromuscular Disorders : NMD|June 1, 2014
Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth diseaseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Neurology|October 17, 2020
Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor NeuropathyHerminia Argente-Escrig, Joshua Burns, Gabrielle Donlevy, et al.
Hip International : the Journal of Clinical and Experimental Research on Hip Pathology and Therapy|June 28, 2021
Reliability and sensitivity of radiographic measures of hip dysplasia in childhood Charcot-Marie-Tooth diseaseLeanne N Dwan, Paul Gibbons, Kamal Jamil, et al.
Journal of Physiotherapy|May 27, 2014
Randomised controlled trial protocol of foot and ankle exercise for children with Charcot-Marie-Tooth diseaseAmy D Sman, Jacqueline Raymond, Kathryn M Refshauge, et al.
Developmental Medicine and Child Neurology|February 27, 2016
Auditory neuropathy in Brown-Vialetto-Van Laere syndrome due to riboflavin transporter RFVT2 deficiencyManoj P Menezes, Katherine O'Brien, Mandy Hill, et al.
Journal of Paediatrics and Child Health|August 24, 2022
Steroid-responsive aseptic meningitis with raised intracranial pressure syndrome associated with myelin oligodendrocyte glycoprotein autoantibodiesWui-Kwan Wong, Christopher Troedson, Ken Peacock, et al.
Journal of the Peripheral Nervous System : JPNS|March 6, 2024
Development of a functional outcome measure for riboflavin transporter deficiencyJack R Fennessy, Gabrielle A Donlevy, Marnee J McKay, et al.
Developmental Medicine and Child Neurology|September 10, 2024
Long-term outcomes in children with riboflavin transporter deficiency and surveillance recommendationsJack R Fennessy, Kayla M D Cornett, Gabrielle A Donlevy, et al.
Neurology|June 10, 2020
Prenusinersen economic and health-related quality of life burden of spinal muscular atrophyGeorgina M Chambers, Stella Nalukwago Settumba, Kate A Carey, et al.
Genes & Diseases|March 22, 2024
<i>C. elegans</i> model of riboflavin transporter deficiency (RTD) disorder reveals deficits in synaptic transmission and movementRamesh K Narayanan, Gonzalo Perez-Siles, Kamila A Marzec, et al.
Neuromuscular Disorders : NMD|June 1, 2014
Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth diseaseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Pageof 7