186 related articles for article (PubMed ID: 26337734)
1. Griscelli Syndrome Type 3: Two New Cases and Review of the Literature.
Nouriel A; Zisquit J; Helfand AM; Anikster Y; Greenberger S
Pediatr Dermatol; 2015; 32(6):e245-8. PubMed ID: 26337734
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A rare pigmentary disorder in two non-identical siblings: Griscelli Syndrome -type 3.
Kaur S; Jindal N; Dayal S; Jain VK; Jairath V; Virdi S
Dermatol Online J; 2014 Jul; 20(7):. PubMed ID: 25046460
[TBL] [Abstract][Full Text] [Related]
4. Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion.
Yılmaz M; Çağdaş D; Grandin V; Altıntaş DU; Tezcan İ; de Saint Basile G; Sanal Ö
Pediatr Allergy Immunol; 2014 Dec; 25(8):817-9. PubMed ID: 25283056
[No Abstract] [Full Text] [Related]
5. Teaching neuroImages: Griscelli syndrome and CNS lymphohistiocytosis.
Saini AG; Nagaraju S; Sahu JK; Rawat A; Vyas S; Singhi P
Neurology; 2014 Apr; 82(14):e122-3. PubMed ID: 24711539
[TBL] [Abstract][Full Text] [Related]
6. [Griscelli syndrome type 3: A new case].
Kassem Youssef H; Ramstein C; Ginglinger E; Chouta Ngaha F; Nojavan H; Michel C
Ann Dermatol Venereol; 2018 Dec; 145(12):785-789. PubMed ID: 30389201
[TBL] [Abstract][Full Text] [Related]
7. Boy with silvery grey hair and immunodeficiency.
Khemka P; Bhattacharyya R; Ray S; Mukherjee M
J Paediatr Child Health; 2016 Apr; 52(4):465. PubMed ID: 27145514
[No Abstract] [Full Text] [Related]
8. Silvery-gray hair in a newborn.
Wong L; Yano S
JAMA; 2012 Aug; 308(6):617-8. PubMed ID: 22871872
[No Abstract] [Full Text] [Related]
9. A case of Griscelli syndrome.
Kerketta JA; Lodh M; Mandal K
Dermatol Online J; 2014 Nov; 20(11):. PubMed ID: 25419745
[TBL] [Abstract][Full Text] [Related]
10. Genetic analysis in three Egyptian patients with Griscelli syndrome Type 1 reveals new nonsense mutations in MYO5A.
Abd Elmaksoud MS; Gomaa NS; Azouz HG; On CNV; Ho CT; Omar TE; McGrath JA; Onoufriadis A
Clin Exp Dermatol; 2020 Aug; 45(6):789-792. PubMed ID: 32275080
[No Abstract] [Full Text] [Related]
11. Heterochromia of the Hair and Eyelashes with Blaschkoid Dyspigmentation.
Dumitrascu CI; Hoss E; Hogeling M
Pediatr Dermatol; 2016; 33(2):e121-2. PubMed ID: 26763866
[TBL] [Abstract][Full Text] [Related]
12. Haemophagocytic lymphohistiocytosis and silvery hair in Griscelli syndrome.
Lipsker D
Br J Haematol; 2016 Oct; 175(1):11. PubMed ID: 27434021
[No Abstract] [Full Text] [Related]
13. Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes.
Gironi LC; Zottarelli F; Savoldi G; Notarangelo LD; Basso ME; Ferrero I; Timeus F; Fagioli F; Maiuri L; Colombo E; Savoia P
Medicina (Kaunas); 2019 Mar; 55(3):. PubMed ID: 30934652
[TBL] [Abstract][Full Text] [Related]
14. Cutaneous granulomas as the presenting manifestation of Griscelli syndrome type 2.
Gotesman R; Ramien M; Armour CM; Pham-Huy A; Kirshen C
Pediatr Dermatol; 2021 Jan; 38(1):194-197. PubMed ID: 32965739
[TBL] [Abstract][Full Text] [Related]
15. Silvery hair with dyschromatosis: Griscelli syndrome type 3 or familial gigantic melanocytosis.
Batrani M; Thole A; Kubba A; Mahajan K
J Cutan Pathol; 2018 Dec; 45(12):918-922. PubMed ID: 30129079
[TBL] [Abstract][Full Text] [Related]
16. Oral features of Griscelli syndrome type II: A rare case report.
Tewari N; Rajwar A; Mathur VP; Chaudhari PK
Spec Care Dentist; 2018 Nov; 38(6):421-425. PubMed ID: 30207398
[TBL] [Abstract][Full Text] [Related]
17. Elejalde syndrome--a melanolysosomal neurocutaneous syndrome: clinical and morphological findings in 7 patients.
Duran-McKinster C; Rodriguez-Jurado R; Ridaura C; de la Luz Orozco-Covarrubias M; Tamayo L; Ruiz-Maldonando R
Arch Dermatol; 1999 Feb; 135(2):182-6. PubMed ID: 10052404
[TBL] [Abstract][Full Text] [Related]
18. A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis.
Grandin V; Sepulveda FE; Lambert N; Al Zahrani M; Al Idrissi E; Al-Mousa H; Almanjomi F; Al-Ghonaium A; K Habazi M; A Alghamdi H; Picard C; Bole-Feysot C; Nitschke P; Ménasché G; de Saint Basile G
Hum Mutat; 2017 Oct; 38(10):1355-1359. PubMed ID: 28585352
[TBL] [Abstract][Full Text] [Related]
19. Seizure as the presenting manifestation in Griscelli syndrome type 2.
Panigrahi I; Suthar R; Rawat A; Behera B
Pediatr Neurol; 2015 May; 52(5):535-8. PubMed ID: 25801174
[TBL] [Abstract][Full Text] [Related]
20. Griscelli syndrome type 2.
Gailson T; Pandit S; Chandrasekaran S
QJM; 2020 Feb; 113(2):137. PubMed ID: 31199490
[No Abstract] [Full Text] [Related]
[Next] [New Search]