Results 171 to 180 of about 6,824 (185)

The Clinical Journey of Patients with Riboflavin Transporter Deficiency Type 2

Journal of Child Neurology, 2020
Fatima Amir, Carrie Atzinger
exaly  

Riboflavin transporter deficiency diagnosed 30 years after onset of symptoms

Neuromuscular Disorders, 2016
A. van der Kooi, B. Jaeger, K. van Spaendonck, A. Bosch   +3 more
openaire   +1 more source

Riboflavin transporter deficiency unmasked by dietary changes

Molecular Genetics and Metabolism
Annet Bosch, Bregje Jaeger, Mirjam Langeveld, Robert Brunkhorst, Felix Disterlmaier, Nicole Wolf   +5 more
openaire   +1 more source

Epidemiology of Riboflavin Transporter Deficiency (RTD)

2017
openaire   +1 more source

Auditory Neuropathy in Riboflavin Transporter Deficiency

2017
openaire   +1 more source

Riboflavin Transporter Deficiency Presentation, Genetics and Treatment

2019
openaire   +1 more source

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B

Human Mutation, 2011
Atsushi Yonezawa, Satohiro Masuda, Ken-ichi Inui   +2 more
exaly  

ANTIMALARIAL EFFECTS OF RIBOFLAVIN DEFICIENCY

Lancet, The, 1985
exaly  

Riboflavin Transporter Deficiency or Brown-Vialetto-Van Laere Syndrome

Enrico Bertini, Claudia Compagnucci, Keith Massey   +2 more
openaire   +1 more source

ASSOCIATION OF PRESENILE CATARACTS WITH HETEROZYGOSITY FOR GALACTOSÆMIC STATES AND WITH RIBOFLAVIN DEFICIENCY

Lancet, The, 1978
exaly