BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

334 related articles for article (PubMed ID: 17676217)

  • 1. Light and scanning electron microscopic examination of hair in Griscelli syndrome.
    Celik HH; Tore H; Tunali S; Tatar I; Aldur MM
    Saudi Med J; 2007 Aug; 28(8):1275-7. PubMed ID: 17676217
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Griscelli syndrome - a case report.
    Manglani M; Adhvaryu K; Seth B
    Indian Pediatr; 2004 Jul; 41(7):734-7. PubMed ID: 15297691
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Usefulness of the skin biopsy as a tool in the diagnosis of silvery hair syndrome.
    Ridaura-Sanz C; Durán-McKinster C; Ruiz-Maldonado R
    Pediatr Dermatol; 2018 Nov; 35(6):780-783. PubMed ID: 30338556
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature.
    Mancini AJ; Chan LS; Paller AS
    J Am Acad Dermatol; 1998 Feb; 38(2 Pt 2):295-300. PubMed ID: 9486701
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Griscelli syndrome type 2; a pediatric case with immunodeficiency.
    Tabatabaie P; Mahjoub F; Cheraghi T; Parvaneh N
    Iran J Allergy Asthma Immunol; 2007 Sep; 6(3):155-7. PubMed ID: 17893437
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene.
    Pastural E; Barrat FJ; Dufourcq-Lagelouse R; Certain S; Sanal O; Jabado N; Seger R; Griscelli C; Fischer A; de Saint Basile G
    Nat Genet; 1997 Jul; 16(3):289-92. PubMed ID: 9207796
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and microscopic hair features of griscelli syndrome associated with asymmetric crying facies in an infant.
    Akcakus M; Koklu E; Narin N; Kose M
    Pediatr Dev Pathol; 2008; 11(1):63-5. PubMed ID: 18237235
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Elejalde syndrome: clinical and histopathological findings in an Egyptian male.
    Afifi HH; Zaki MS; El-Kamah GY; El-Darouti M
    Genet Couns; 2007; 18(2):179-88. PubMed ID: 17710870
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two genes are responsible for Griscelli syndrome at the same 15q21 locus.
    Pastural E; Ersoy F; Yalman N; Wulffraat N; Grillo E; Ozkinay F; Tezcan I; Gediköglu G; Philippe N; Fischer A; de Saint Basile G
    Genomics; 2000 Feb; 63(3):299-306. PubMed ID: 10704277
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Trichorrhexis congenita. Scanning electron microscopic studies on a congenital disorder of hair growth].
    Wolff HH; Vigl E; Braun-Falco O
    Hautarzt; 1975 Nov; 26(11):576-80. PubMed ID: 1205844
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Griscelli syndrome in a Mexican girl].
    Ayala de la Cruz Mdel C; Ramírez Campos J; Govea Sifuentes J; González Cabello D; Calderón Garcidueñas AL; Moreno L; Vargas Almanza GN
    Rev Alerg Mex; 2002; 49(1):16-9. PubMed ID: 12070892
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Silvery grey hair: clue to diagnose immunodeficiency.
    Sahana M; Sacchidanand S; Hiremagalore R; Asha G
    Int J Trichology; 2012 Apr; 4(2):83-5. PubMed ID: 23180914
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The Griscelli-Prunieras syndrome: a case report].
    Salazar-Cabrera AN; Matos-Martínez M; Sánchez-Villegas MC; Lázaro-Castillo LM; Méndez-León J; Martínez-Amigon J; Aguilar M; García-Escobar B
    Bol Med Hosp Infant Mex; 1993 Jul; 50(7):503-7. PubMed ID: 8363750
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre.
    Smith VV; Anderson G; Malone M; Sebire NJ
    J Clin Pathol; 2005 Dec; 58(12):1294-8. PubMed ID: 16311350
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Monilethrix. Comparative scanning electron microscopic study of the hair in one family.
    Lubach D; Glowienka F; Castellucci M
    Dermatologica; 1982 Jan; 164(1):1-9. PubMed ID: 7067874
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Light and scanning electron microscopic examination of late changes in hair with hereditary trichodysplasia (Marie Unna hypotrichosis).
    Celik HH; Surucu SH; Aldur MM; Ozdemir BM; Karaduman AA; Cumhur MM
    Saudi Med J; 2004 Nov; 25(11):1648-51. PubMed ID: 15573195
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Griscelli syndrome.
    Malhotra AK; Bhaskar G; Nanda M; Kabra M; Singh MK; Ramam M
    J Am Acad Dermatol; 2006 Aug; 55(2):337-40. PubMed ID: 16844525
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Griscelli syndrome type 2: A rare and fatal syndrome in a South Indian boy.
    Rajyalakshmi R; Chakrapani RN
    Indian J Pathol Microbiol; 2016; 59(1):113-6. PubMed ID: 26960655
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Accelerated phase in partial albinism with immunodeficiency (Griscelli syndrome): genetics and stem cell transplantation in a 2-month-old girl.
    Baumeister FA; Stachel D; Schuster F; Schmid I; Schaller M; Wolff H; Weiss M; Belohradsky BH
    Eur J Pediatr; 2000; 159(1-2):74-8. PubMed ID: 10653334
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A hemophagocytic syndrome revealing a Griscelli syndrome type 2].
    Jennane S; El Kababri M; Hessissen L; Kili A; Nachef MN; Messaoudi N; Doghmi K; Mikdame M; El Khorassani M; Khattab M
    Ann Biol Clin (Paris); 2013; 71(4):461-4. PubMed ID: 23906575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.