Compounds > biotin
Page last updated: 2024-09-05

biotin and Amyotonia Congenita

biotin has been researched along with Amyotonia Congenita in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's2 (66.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Agroyannis, B; Delatola, Z; Francos-Plemenos, M; Koutsicos, D; Papastephanidis, C; Yatzidis, H1
Kawai, H; Mitsui, T; Naruo, T; Nishino, H; Saito, S1
Campos-Castelló, J; Careaga Maldonado, J; Casado de Frías, E; Pérez Cerdá, C1

Other Studies

3 other study(ies) available for biotin and Amyotonia Congenita

ArticleYear
Biotin in the management of uremic neurologic disorders.
    Nephron, 1984, Volume: 36, Issue:3

    Topics: Biotin; Dementia; Humans; Neuromuscular Diseases; Peripheral Nervous System Diseases; Renal Dialysis; Uremia

1984
In situ hybridization of myoglobin mRNA: results on the skeletal muscles of normal subjects and patients with neuromuscular diseases.
    Acta neuropathologica, 1993, Volume: 86, Issue:4

    Topics: Adult; Alkaline Phosphatase; Amyotrophic Lateral Sclerosis; Biotin; Child; Densitometry; Female; Humans; In Situ Hybridization; Male; Middle Aged; Muscles; Muscular Dystrophies; Myoglobin; Neuromuscular Diseases; RNA, Messenger

1993
Biotinidase deficiency: result of treatment with biotin from age 12 years.
    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 1997, Volume: 1, Issue:5-6

    Topics: Amidohydrolases; Biotin; Biotinidase; Brain; Child; Humans; Magnetic Resonance Imaging; Male; Multiple Carboxylase Deficiency; Neuromuscular Diseases; Spinal Cord; Treatment Outcome

1997