BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 2189905)

  • 21. A new case of trichothiodystrophy associated with autism, seizures, and mental retardation.
    Schepis C; Elia M; Siragusa M; Barbareschi M
    Pediatr Dermatol; 1997; 14(2):125-8. PubMed ID: 9144699
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Family with "pure" hair-nail ectodermal dysplasia.
    Barbareschi M; Cambiaghi S; Crupi AC; Tadini G
    Am J Med Genet; 1997 Oct; 72(1):91-3. PubMed ID: 9295083
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Loose anagen hair in hypohidrotic ectodermal dysplasia.
    Azon-Masoliver A; Ferrando J
    Pediatr Dermatol; 1996; 13(1):29-32. PubMed ID: 8919521
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A new variant of trichothiodystrophy with recurrent infections, failure to thrive, and death.
    Petrin JH; Meckler KA; Sybert VP
    Pediatr Dermatol; 1998; 15(1):31-4. PubMed ID: 9496800
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
    Itin PH; Sarasin A; Pittelkow MR
    J Am Acad Dermatol; 2001 Jun; 44(6):891-920; quiz 921-4. PubMed ID: 11369901
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.
    Naeem M; Wajid M; Lee K; Leal SM; Ahmad W
    J Med Genet; 2006 Mar; 43(3):274-9. PubMed ID: 16525032
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature.
    Civitelli R; McAlister WH; Teitelbaum SL; Whyte MP
    J Bone Miner Res; 1989 Dec; 4(6):863-75. PubMed ID: 2692405
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Trichothiodystrophy with severe cardiac and neurological involvement in two sisters.
    Toelle SP; Valsangiacomo E; Boltshauser E
    Eur J Pediatr; 2001 Dec; 160(12):728-31. PubMed ID: 11795681
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.
    Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N
    Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Trichothiodystrophy.
    Milligan A; Fletcher A; Porter DI; Hutchinson PE
    Clin Exp Dermatol; 1991 Jul; 16(4):264-7. PubMed ID: 1794166
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Diagnosis of trichothiodystrophy in 2 siblings.
    Bracun R; Hemmer W; Wolf-Abdolvahab S; Focke M; Botzi C; Killian W; Götz M; Jarisch R
    Dermatology; 1997; 194(1):74-6. PubMed ID: 9031799
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Trichothiodystrophy].
    Meynadier J; Guillot B; Barnéon G; Djian B; Lévy A
    Ann Dermatol Venereol; 1987; 114(12):1529-36. PubMed ID: 3445983
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.
    Stefanini M; Lagomarsini P; Giorgi R; Nuzzo F
    Mutat Res; 1987 Jun; 191(2):117-9. PubMed ID: 3600693
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Towards a new classification of ectodermal dysplasias.
    Lamartine J
    Clin Exp Dermatol; 2003 Jul; 28(4):351-5. PubMed ID: 12823289
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Hair anomalies in syndromic disorders].
    Frank J; Betz RC
    Hautarzt; 2019 Jul; 70(7):514-519. PubMed ID: 31197391
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Tay syndrome (congenital ichthyosis with trichothiodystrophy).
    Happle R; Traupe H; Gröbe H; Bonsmann G
    Eur J Pediatr; 1984 Jan; 141(3):147-52. PubMed ID: 6538137
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Central osteosclerosis with trichothiodystrophy.
    Wakeling EL; Cruwys M; Suri M; Brady AF; Aylett SE; Hall C
    Pediatr Radiol; 2004 Jul; 34(7):541-6. PubMed ID: 15148554
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure.
    Lucky PA; Kirsch N; Lucky AW; Carter DM
    J Am Acad Dermatol; 1984 Aug; 11(2 Pt 2):340-6. PubMed ID: 6480939
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Trichoscopy in Hair Shaft Disorders.
    Rudnicka L; Olszewska M; Waśkiel A; Rakowska A
    Dermatol Clin; 2018 Oct; 36(4):421-430. PubMed ID: 30201151
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Trichothiodystrophy type 4 in an Indian family.
    Pande S; Shukla A; Girisha KM
    Am J Med Genet A; 2020 Oct; 182(10):2226-2229. PubMed ID: 33043633
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.