Page last updated: 2024-08-21

d-alpha tocopherol and Autosomal Dominant Cerebellar Ataxia, Type II

d-alpha tocopherol has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bellayou, H; Bourezgui, M; Dehbi, H; Nadifi, S; Slassi, I	1
Chaudhry, N; Prakash, V; Puri, V; Tatke, M	1

Other Studies

2 other study(ies) available for d-alpha tocopherol and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Ataxia with vitamin E deficiency (AVED); an example of the contribution of research in molecular genetic to counselling in Morocco. Pathologie-biologie, 2009, Volume: 57, Issue:5 Topics: Carrier Proteins; Chromosomes, Human, Pair 8; Consanguinity; Deoxyribonucleases, Type II Site-Specific; DNA Mutational Analysis; Female; Genetic Counseling; Genetic Testing; Humans; Intestinal Absorption; Male; Morocco; Polymorphism, Restriction Fragment Length; Prevalence; Sequence Deletion; Spinocerebellar Ataxias; Vitamin E; Vitamin E Deficiency	2009
Isolated vitamin E deficiency with demyelinating neuropathy. Muscle & nerve, 2005, Volume: 32, Issue:2 Topics: Adult; Biopsy; Demyelinating Diseases; Electrodiagnosis; Humans; Male; Muscle Weakness; Muscular Atrophy; Nerve Fibers, Myelinated; Neural Conduction; Peripheral Nerves; Peripheral Nervous System Diseases; Seizures; Somatosensory Disorders; Spinocerebellar Ataxias; Sural Nerve; Vitamin E; Vitamin E Deficiency	2005

Article

Year

Ataxia with vitamin E deficiency (AVED); an example of the contribution of research in molecular genetic to counselling in Morocco.

Pathologie-biologie, 2009, Volume: 57, Issue:5

Topics: Carrier Proteins; Chromosomes, Human, Pair 8; Consanguinity; Deoxyribonucleases, Type II Site-Specific; DNA Mutational Analysis; Female; Genetic Counseling; Genetic Testing; Humans; Intestinal Absorption; Male; Morocco; Polymorphism, Restriction Fragment Length; Prevalence; Sequence Deletion; Spinocerebellar Ataxias; Vitamin E; Vitamin E Deficiency

2009

Isolated vitamin E deficiency with demyelinating neuropathy.

Muscle & nerve, 2005, Volume: 32, Issue:2

Topics: Adult; Biopsy; Demyelinating Diseases; Electrodiagnosis; Humans; Male; Muscle Weakness; Muscular Atrophy; Nerve Fibers, Myelinated; Neural Conduction; Peripheral Nerves; Peripheral Nervous System Diseases; Seizures; Somatosensory Disorders; Spinocerebellar Ataxias; Sural Nerve; Vitamin E; Vitamin E Deficiency

2005