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 *

93 related articles for article (PubMed ID: 6824580)

  • 41. Friable hair, urea cycle dysfunction, and trichothiodystrophy. A new X-linked genodermatosis.
    Hordinsky MK; Briden B; Berry SA
    Curr Probl Dermatol; 1987; 17():52-60. PubMed ID: 3595193
    [No Abstract]   [Full Text] [Related]  

  • 42. Trichothiodystrophy and the relationship between DNA repair and cancer.
    Lehmann AR
    Bioessays; 1989 Dec; 11(6):168-70. PubMed ID: 2695082
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Ocular manifestations of genetic skin disorders.
    Jen M; Nallasamy S
    Clin Dermatol; 2016; 34(2):242-75. PubMed ID: 26903188
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Syndromes associated with trichothiodystrophy.
    Tolmie JL; de Berker D; Dawber R; Galloway C; Gregory DW; Lehmann AR; McClure J; Pollitt RJ; Stephenson JB
    Clin Dysmorphol; 1994 Jan; 3(1):1-14. PubMed ID: 8205320
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Severe hypernatremic dehydration disclosing Netherton syndrome in the neonatal period].
    Giroux JD; Sizun J; Gardach C; Awad H; Guillois B; Alix D
    Arch Fr Pediatr; 1993; 50(7):585-8. PubMed ID: 8002723
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Nucleotide excision repair syndromes: molecular basis and clinical symptoms.
    Bootsma D; Weeda G; Vermeulen W; van Vuuren H; Troelstra C; van der Spek P; Hoeijmakers J
    Philos Trans R Soc Lond B Biol Sci; 1995 Jan; 347(1319):75-81. PubMed ID: 7746858
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities.
    Rasheed M; Shahzad S; Zaeem A; Afzal I; Gul A; Khalid S
    Arch Dermatol Res; 2017 Dec; 309(10):773-785. PubMed ID: 28913623
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. 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]  

  • 50. Accelerated bone aging in the trichothiodystrophy mouse model.
    Diderich KE; Hoeijmakers JH; van Leeuwen JP
    J Gerontol A Biol Sci Med Sci; 2003 Nov; 58(11):969. PubMed ID: 14630875
    [No Abstract]   [Full Text] [Related]  

  • 51. Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases.
    King MD; Gummer CL; Stephenson JB
    J Med Genet; 1984 Aug; 21(4):286-9. PubMed ID: 6492094
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Trichothiodystrophy: report of a new case with severe nervous system impairment.
    Rizzo R; Pavone L; Micali G; Calvieri S; Di Gregorio L
    J Child Neurol; 1992 Jul; 7(3):300-3. PubMed ID: 1634754
    [No Abstract]   [Full Text] [Related]  

  • 53. Rough skin, brittle hair, and photosensitivity: a mild phenotypic variant of trichothiodystrophy.
    Savarirayan R; Gardner RJ; Sinclair RD; McDowell M; Cleaver JE
    J Med Genet; 2000 Apr; 37(4):312-4. PubMed ID: 10819642
    [No Abstract]   [Full Text] [Related]  

  • 54. [Trichothiodystrophy. Hair examination as a diagnostic tool].
    Hansen LK; Wulff K; Brandrup F
    Ugeskr Laeger; 1993 Jun; 155(25):1949-52. PubMed ID: 8317059
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Cerebellar and cerebral atrophy in trichothiodystrophy.
    Yoon HK; Sargent MA; Prendiville JS; Poskitt KJ
    Pediatr Radiol; 2005 Oct; 35(10):1019-23. PubMed ID: 15912410
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Cuticle cell defects in lamellar ichthyosis hair and anomalous hair shaft syndromes visualized after detergent extraction.
    Rice RH; Wong VJ; Price VH; Hohl D; Pinkerton KE
    Anat Rec; 1996 Dec; 246(4):433-40. PubMed ID: 8955782
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature (IBIDS syndrome).
    Jorizzo JL; Atherton DJ; Crounse RG; Wells RS
    Br J Dermatol; 1982 Jun; 106(6):705-10. PubMed ID: 7082576
    [No Abstract]   [Full Text] [Related]  

  • 58. A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
    Cleaver JE; Thompson LH; Richardson AS; States JC
    Hum Mutat; 1999; 14(1):9-22. PubMed ID: 10447254
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A girl with photosensitivity and hepatic steatosis.
    Pavan M; Gortani G; Rubinato E; Faletra F; Pastore S; Ventura A
    J Pediatr; 2014 Jul; 165(1):201-201.e1. PubMed ID: 24704299
    [No Abstract]   [Full Text] [Related]  

  • 60. Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships.
    Botta E; Offman J; Nardo T; Ricotti R; Zambruno G; Sansone D; Balestri P; Raams A; Kleijer WJ; Jaspers NG; Sarasin A; Lehmann AR; Stefanini M
    Hum Mutat; 2007 Jan; 28(1):92-6. PubMed ID: 16977596
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.