These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 8779325)

  • 1. 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]  

  • 2. Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females.
    Al-Awadi SA; Farag TI; Teebi AS; Naguib K; el-Khalifa MY; Kelani Y; Al-Ansari A; Schimke RN
    Am J Med Genet; 1985 Nov; 22(3):619-22. PubMed ID: 4061495
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome.
    Ali RH; Shah K; Nasir A; Steyaert W; Coucke PJ; Ahmad W
    Clin Genet; 2016 Sep; 90(3):263-9. PubMed ID: 26612766
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature.
    Agopiantz M; Corbonnois P; Sorlin A; Bonnet C; Klein M; Hubert N; Pascal-Vigneron V; Jonveaux P; Cuny T; Leheup B; Weryha G
    J Endocrinol Invest; 2014 Jan; 37(1):1-7. PubMed ID: 24464444
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
    Tipton RE; Gorlin RJ
    Am J Med Genet; 1984 Oct; 19(2):209-16. PubMed ID: 6507471
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism.
    Johnson VP; McMillin JM; Aceto T; Bruins G
    Am J Med Genet; 1983 Jul; 15(3):497-506. PubMed ID: 6881216
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Aicardi-Goutières syndrome: an expanding phenotype.
    McEntagart M; Kamel H; Lebon P; King MD
    Neuropediatrics; 1998 Jun; 29(3):163-7. PubMed ID: 9706629
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A newly recognized partial alopecia syndrome associated with distinct personality traits.
    Straussberg R; Regenbogen L; Goodman RM
    J Craniofac Genet Dev Biol; 1991; 11(1):3-6. PubMed ID: 2061403
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome.
    Almeqdadi M; Kemppainen JL; Pichurin PN; Gavrilova RH
    Am J Case Rep; 2018 Mar; 19():347-353. PubMed ID: 29574468
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical Reasoning: Seven-year-old girl with progressive gait difficulties.
    Alderson J; Ghosh PS
    Neurology; 2020 Feb; 94(8):364-367. PubMed ID: 32033986
    [No Abstract]   [Full Text] [Related]  

  • 17. Ophthalmic aspects of GAPO syndrome: case report and review.
    Rim PH; Marques-de-Faria AP
    Ophthalmic Genet; 2005 Sep; 26(3):143-7. PubMed ID: 16272061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene.
    Shah K; Jan A; Ahmad F; Basit S; Ramzan K; Ahmad W
    Clin Exp Dermatol; 2020 Mar; 45(2):159-164. PubMed ID: 31323129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene.
    Ben-Omran T; Ali R; Almureikhi M; Alameer S; Al-Saffar M; Walsh CA; Felie JM; Teebi A
    Am J Med Genet A; 2011 Nov; 155A(11):2647-53. PubMed ID: 21964978
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Extrapyramidal symptoms in Wilson's disease are associated with olfactory dysfunction.
    Mueller A; Reuner U; Landis B; Kitzler H; Reichmann H; Hummel T
    Mov Disord; 2006 Sep; 21(9):1311-6. PubMed ID: 16763975
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.