268 related articles for article (PubMed ID: 18175354)
1. Dystonia in the Woodhouse Sakati syndrome: A new family and literature review.
Schneider SA; Bhatia KP
Mov Disord; 2008 Mar; 23(4):592-6. PubMed ID: 18175354
[TBL] [Abstract][Full Text] [Related]
2. Woodhouse-Sakati syndrome: case report and symptoms review.
Medica I; Sepcić J; Peterlin B
Genet Couns; 2007; 18(2):227-31. PubMed ID: 17710875
[TBL] [Abstract][Full Text] [Related]
3. Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene.
Nanda A; Pasternack SM; Mahmoudi H; Ishorst N; Grimalt R; Betz RC
Pediatr Dermatol; 2014; 31(1):83-7. PubMed ID: 24015686
[TBL] [Abstract][Full Text] [Related]
4. Woodhouse-Sakati syndrome in an Israeli-Arab family presenting with youth-onset diabetes mellitus and delayed puberty.
Rachmiel M; Bistritzer T; Hershkoviz E; Khahil A; Epstein O; Parvari R
Horm Res Paediatr; 2011; 75(5):362-6. PubMed ID: 21304230
[TBL] [Abstract][Full Text] [Related]
5. Woodhouse-Sakati Syndrome: First report of a Portuguese case.
Louro P; Durães J; Oliveira D; Paiva S; Ramos L; Macário MC
Am J Med Genet A; 2019 Nov; 179(11):2237-2240. PubMed ID: 31347785
[TBL] [Abstract][Full Text] [Related]
6. Patterns of neurological manifestations in Woodhouse-Sakati Syndrome.
Bohlega S; Abusrair AH; Al-Ajlan FS; Alharbi N; Al-Semari A; Bohlega B; Abualsaud D; Alkuraya F
Parkinsonism Relat Disord; 2019 Dec; 69():99-103. PubMed ID: 31726291
[TBL] [Abstract][Full Text] [Related]
7. Two cases of autosomal recessive generalized dystonia in childhood: 5 year follow-up and bilateral globus pallidus stimulation results.
Lenders MW; Vergouwen MD; Hageman G; van der Hoek JA; Ippel EF; Jansen Steur EN; Buschman HP; Hariz M
Eur J Paediatr Neurol; 2006 Jan; 10(1):5-9. PubMed ID: 16439172
[TBL] [Abstract][Full Text] [Related]
8. Brain MR Imaging Findings in Woodhouse-Sakati Syndrome.
Abusrair AH; Bohlega S; Al-Semari A; Al-Ajlan FS; Al-Ahmadi K; Mohamed B; AlDakheel A
AJNR Am J Neuroradiol; 2018 Dec; 39(12):2256-2262. PubMed ID: 30409855
[TBL] [Abstract][Full Text] [Related]
9. Persistent extrapyramidal syndrome with dystonia and rigidity caused by combined metoclopramide and prochlorperazine therapy.
Factor SA; Matthews MK
South Med J; 1991 May; 84(5):626-8. PubMed ID: 2035085
[TBL] [Abstract][Full Text] [Related]
10. Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1.
Al-Semari A; Bohlega S
Am J Med Genet A; 2007 Jan; 143A(2):149-60. PubMed ID: 17167799
[TBL] [Abstract][Full Text] [Related]
11. [A case of juvenile onset ataxia with dystonia, myoclonus, sensorineural hearing loss and mental retardation].
Koide R; Yoshimura N; Soma Y; Tsuji S
Rinsho Shinkeigaku; 1993 Aug; 33(8):909-11. PubMed ID: 8261707
[TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene.
Binder J; Hofmann S; Kreisel S; Wöhrle JC; Bäzner H; Krauss JK; Hennerici MG; Bauer MF
Brain; 2003 Aug; 126(Pt 8):1814-20. PubMed ID: 12805099
[TBL] [Abstract][Full Text] [Related]
13. Woodhouse-Sakati Syndrome Presenting With Psychotic Features After Starting Trihexyphenidyl: A Case Report.
Aljaffer MA; Almadani AH; AlMutlaq M; Alhammad A; Alyahya AS
Cureus; 2022 Aug; 14(8):e27576. PubMed ID: 36059322
[TBL] [Abstract][Full Text] [Related]
14. Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.
Fozia F; Shah K; Nazli R; Khan SA; Ahmad I; Mohammad N; Khan S; Alotaibi A
J Clin Lab Anal; 2022 Jan; 36(1):e24127. PubMed ID: 34877714
[TBL] [Abstract][Full Text] [Related]
15. A novel splice site mutation in gene C2orf37 underlying Woodhouse-Sakati syndrome (WSS) in a consanguineous family of Pakistani origin.
Habib R; Basit S; Khan S; Khan MN; Ahmad W
Gene; 2011 Dec; 490(1-2):26-31. PubMed ID: 21963443
[TBL] [Abstract][Full Text] [Related]
16. Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?
Devriendt K; Legius E; Fryns JP
Am J Med Genet; 1996 Mar; 62(1):54-7. PubMed ID: 8779325
[TBL] [Abstract][Full Text] [Related]
17. Pili torti and sensorineural hearing loss. A follow-up of Bjørnstad's original patients and a review of the literature.
Selvaag E
Eur J Dermatol; 2000 Mar; 10(2):91-7. PubMed ID: 10694305
[TBL] [Abstract][Full Text] [Related]
18. Two siblings with Allgrove's syndrome and extrapyramidal features.
Jacob A; Parameswaran K; Kishore A
Neurol India; 2003 Jun; 51(2):257-9. PubMed ID: 14571020
[TBL] [Abstract][Full Text] [Related]
19. Clinical spectrum of Hallervorden-Spatz syndrome in India.
Sachin S; Goyal V; Singh S; Shukla G; Sharma MC; Gaikwed S; Behari M
J Clin Neurosci; 2009 Feb; 16(2):253-8. PubMed ID: 19056277
[TBL] [Abstract][Full Text] [Related]
20. Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation.
Hdiji O; Turki E; Bouzidi N; Bouchhima I; Damak M; Bohlega S; Mhiri C
J Mov Disord; 2016 May; 9(2):120-3. PubMed ID: 27240811
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]