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Brain, ISSN 0006-8950, 2014, Volume 137, Issue 1, pp. 44 - 56
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of disorders. A particularly severe subgroup first described in... 
Brown-Vialetto-Van Laere syndrome | RFVT2 | riboflavin therapy | childhood neuronopathy | SLC52A2 | VIALETTO-VAN-LAERE | PONTOBULBAR PALSY | VANLAERE SYNDROME | AUTOSOMAL RECESSIVE INHERITANCE | FAZIO-LONDE-DISEASE | PROGRESSIVE BULBAR PARALYSIS | NEUROSCIENCES | CLINICAL NEUROLOGY | FAMILY | OVERLAP | DEAFNESS | BRAIN | Ataxia | Original
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 08/2016, Volume 58, Issue 8, pp. 848 - 854
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 2011, Volume 34, Issue 1, pp. 159 - 164
Journal Article
The Journal of Biochemistry, ISSN 0021-924X, 10/2011, Volume 150, Issue 4, pp. 341 - 343
Riboflavin or vitamin B2 is one of the constituents of energy drinks. Although this compound is known to be absorbed in the intestine and that it circulates... 
Riboflavin | Absorption | Intestine | Transporter | Energy drink | CELLS | MECHANISM | INVITRO | BIOCHEMISTRY & MOLECULAR BIOLOGY | RAT SMALL-INTESTINE | FUNCTIONAL-CHARACTERIZATION | BORDER MEMBRANE-VESICLES | Membrane Transport Proteins - metabolism | Animals | Humans | Riboflavin - metabolism
Journal Article
Journal Article
The FEBS Journal, ISSN 1742-464X, 02/2007, Volume 274, Issue 3, pp. 612 - 629
Secondary transmembrane transport carriers fall into families and superfamilies allowing prediction of structure and function. Here we describe hundreds of... 
cyclic di‐GMP metabolism | regulation | bile acids | topology | arsenite | secondary carriers | transporter | phylogeny | intragenic duplication | riboflavin | Bile acids | Cyclic di-GMP metabolism | Secondary carriers | Intragenic duplication | Riboflavin | Regulation | Phylogeny |