306 related articles for article (PubMed ID: 9760855)
1. [Ataxia due to vitamin E deficiency].
Gjerde IO; Storstein A; Skeie GO; Wester K; Hegrestad S; Houge G
Tidsskr Nor Laegeforen; 1998 Aug; 118(20):3126-8. PubMed ID: 9760855
[TBL] [Abstract][Full Text] [Related]
2. [Therapeutic developments in chronic ataxias].
Buompadre MC
Medicina (B Aires); 2013; 73 Suppl 1():49-54. PubMed ID: 24072051
[TBL] [Abstract][Full Text] [Related]
3. Correlation between neurological dysfunction with vitamin E deficiency and gastrectomy.
Ueda N; Suzuki Y; Rino Y; Takahashi T; Imada T; Takanashi Y; Kuroiwa Y
J Neurol Sci; 2009 Dec; 287(1-2):216-20. PubMed ID: 19709675
[TBL] [Abstract][Full Text] [Related]
4. Spinocerebellar degeneration secondary to chronic intestinal malabsorption: a vitamin E deficiency syndrome.
Harding AE; Muller DP; Thomas PK; Willison HJ
Ann Neurol; 1982 Nov; 12(5):419-24. PubMed ID: 7181449
[TBL] [Abstract][Full Text] [Related]
5. Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.
Marzouki N; Benomar A; Yahyaoui M; Birouk N; Elouazzani M; Chkili T; Benlemlih M
Eur J Med Genet; 2005; 48(1):21-8. PubMed ID: 15953402
[TBL] [Abstract][Full Text] [Related]
6. [Neurological symptoms associated with vitamin E deficiency].
Sela BA; Shorer Z; Doolman R; Yahav Y; Brill G; Carmi R; Shahar E
Harefuah; 1995 Dec; 129(12):539-42, 615. PubMed ID: 8682350
[TBL] [Abstract][Full Text] [Related]
7. [Friedreich's ataxia and hereditary vitamin E deficiency. Case study].
Labauge P; Cavalier L; Ichalalène L; Castelnovo G
Rev Neurol (Paris); 1998 May; 154(4):339-41. PubMed ID: 9773063
[TBL] [Abstract][Full Text] [Related]
8. Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.
Mariotti C; Gellera C; Rimoldi M; Mineri R; Uziel G; Zorzi G; Pareyson D; Piccolo G; Gambi D; Piacentini S; Squitieri F; Capra R; Castellotti B; Di Donato S
Neurol Sci; 2004 Jul; 25(3):130-7. PubMed ID: 15300460
[TBL] [Abstract][Full Text] [Related]
9. [Ataxia with isolated vitamin E deficiency].
Saito Y; Yokota T
Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):218-20. PubMed ID: 10434635
[No Abstract] [Full Text] [Related]
10. First case of ataxia with isolated vitamin E deficiency in the Netherlands.
Ponten SC; Kwee ML; Wolters ECh; Zijlmans JC
Parkinsonism Relat Disord; 2007 Jul; 13(5):315-6. PubMed ID: 17049453
[TBL] [Abstract][Full Text] [Related]
11. Spinocerebellar degeneration associated with a selective defect of vitamin E absorption.
Harding AE; Matthews S; Jones S; Ellis CJ; Booth IW; Muller DP
N Engl J Med; 1985 Jul; 313(1):32-5. PubMed ID: 4000224
[No Abstract] [Full Text] [Related]
12. Ataxia with vitamin E deficiency associated with deafness.
Kara B; Uzümcü A; Uyguner O; Rosti RO; Koçbaş A; Ozmen M; Kayserili H
Turk J Pediatr; 2008; 50(5):471-5. PubMed ID: 19102053
[TBL] [Abstract][Full Text] [Related]
13. [Gait ataxia in short bowel syndrome: vitamin E deficiency syndrome].
Graepler F; Gregor M; Riecken EO
Med Klin (Munich); 1992 Nov; 87(11):602-7. PubMed ID: 1470060
[No Abstract] [Full Text] [Related]
14. Normal spermatogenesis and sperm function in a subject affected by cerebellar ataxia due to congenital vitamin E deficiency.
Rossato M; Mariotti C
Andrologia; 2014 Apr; 46(3):322-4. PubMed ID: 23445347
[TBL] [Abstract][Full Text] [Related]
15. [A patient with vitamin E deficient, myopathy presenting with amyotrophy].
Osoegawa M; Ohyagi Y; Inoue I; Tsuruta Y; Iwaki T; Taniwaki T; Kira J
Rinsho Shinkeigaku; 2001 Jul; 41(7):428-31. PubMed ID: 11808355
[TBL] [Abstract][Full Text] [Related]
16. [Chronic polyneuropathy due to vitamin E deficiency].
Ayuso Blanco T; Martín Martínez J; Figueras P; Velilla Marco J; Monzón Monguilod MJ
Neurologia; 1994; 9(7):300-2. PubMed ID: 7946427
[TBL] [Abstract][Full Text] [Related]
17. Cerebellar syndrome in adult celiac disease with vitamin E deficiency.
Mauro A; Orsi L; Mortara P; Costa P; Schiffer D
Acta Neurol Scand; 1991 Aug; 84(2):167-70. PubMed ID: 1950453
[TBL] [Abstract][Full Text] [Related]
18. Disappearance of skin lipofuscin storage and marked clinical improvement in adult onset coeliac disease and severe vitamin E deficiency after chronic vitamin E megatherapy.
Battisti C; Dotti MT; Formichi P; Bonuccelli U; Malandrini A; Carrai M; Tripodi SA; Federico A
J Submicrosc Cytol Pathol; 1996 Jul; 28(3):339-44. PubMed ID: 8765578
[TBL] [Abstract][Full Text] [Related]
19. Thiamine deficiency: a cause of childhood ataxia not to be ignored.
Ogunlesi TA
Ann Trop Paediatr; 2004 Dec; 24(4):357-60. PubMed ID: 15720894
[TBL] [Abstract][Full Text] [Related]
20. A novel delins mutation in the alpha-TTP gene in a family segregating ataxia with isolated vitamin E deficiency.
Fernández-Burriel M; Martínez-Rubio D; Lupo V; Pérez-Colosía V; Piñán-López E; Palau F; Espinós C
Pediatr Res; 2008 Sep; 64(3):262-4. PubMed ID: 18458655
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]