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.
110 related articles for article (PubMed ID: 10564887)
1. Is there a relationship between extensive mongolian spots and inborn errors of metabolism? Silengo M; Battistoni G; Spada M Am J Med Genet; 1999 Nov; 87(3):276-7. PubMed ID: 10564887 [No Abstract] [Full Text] [Related]
2. Extensive Mongolian spots: a clinical sign merits special attention. Ashrafi MR; Shabanian R; Mohammadi M; Kavusi S Pediatr Neurol; 2006 Feb; 34(2):143-5. PubMed ID: 16458829 [TBL] [Abstract][Full Text] [Related]
3. Mongolian spots in the newborn: do they mean anything? Snow TM Neonatal Netw; 2005; 24(1):31-3. PubMed ID: 15717433 [TBL] [Abstract][Full Text] [Related]
4. Extensive irregular Mongolian blue spots as a clue for GM1 gangliosidosis type 1. Bersani G; Guerriero C; Ricci F; Valentini P; Zampino G; Lazzareschi I; Antuzzi D; Rigante D J Dtsch Dermatol Ges; 2016 Mar; 14(3):301-2. PubMed ID: 26765271 [No Abstract] [Full Text] [Related]
6. Atypical mongolian spots as the initial manifestation of a lysosomal storage disorder. Demirel Öğüt N; Akdoğan N; Ateş Özdemir D; Akın MŞ; Isıyel E; Ersoy Evans S Australas J Dermatol; 2020 Aug; 61(3):e371-e373. PubMed ID: 32173853 [No Abstract] [Full Text] [Related]
7. Mongolian spots in GM1 gangliosidosis: a pictorial report. Mishra S; Pai P; Uttarilli A; Girisha KM Clin Dysmorphol; 2021 Jan; 30(1):6-9. PubMed ID: 33038107 [TBL] [Abstract][Full Text] [Related]
8. [Extensive mongolian spot: a clinical sign that deserves attention]. Abilkassem R; Agadr A Pan Afr Med J; 2013; 16():41. PubMed ID: 24648854 [No Abstract] [Full Text] [Related]
9. A 6-week-old girl with generalized edema of unknown etiology. Listernick R Pediatr Ann; 2014 Apr; 43(4):125-8. PubMed ID: 24716554 [No Abstract] [Full Text] [Related]
10. Coincidental GM1 gangliosidosis in an infant with alpha-1-antitrypsin deficiency. Srinivasan R; Sudeendra S; Cosgrove M; Wagner B; Baker AJ; Portmann B J Pediatr Gastroenterol Nutr; 2008 Aug; 47(2):196-8. PubMed ID: 18664873 [No Abstract] [Full Text] [Related]
11. [Ocular manifestations of patients with gangliosidosis]. Fei P; Qin M; Hu T Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1994 Aug; 16(4):285-9. PubMed ID: 7867097 [TBL] [Abstract][Full Text] [Related]
12. Extensive and Progressing Congenital Dermal Melanocytosis Leading to Diagnosis of GM1 Gangliosidosis. Vedak P; Sells R; De Souza A; Hoang MP; Kroshinsky D Pediatr Dermatol; 2015; 32(6):e294-5. PubMed ID: 26337817 [TBL] [Abstract][Full Text] [Related]
13. [Non-neurological characteristics of Gm1 gangliosidosis type 1. A report of three cases within the same family]. Bernal Ferrer A; Martí Barranco E; Tomás Vila M; Oltra Benavent M; Martinez Martinez J; Chabás A An Esp Pediatr; 1999 May; 50(5):513-6. PubMed ID: 10394196 [No Abstract] [Full Text] [Related]
15. [GM1 syndrome, generalized infantile gangliosidosis. Presentation of two cases]. Alvarez-Valiente H; Cuervo N; Dorado J; Menéndez C Rev Neurol; 1999 May 1-15; 28(9):926-8. PubMed ID: 10390761 [No Abstract] [Full Text] [Related]
16. Infantile form GM1 gangliosidosis with dilated cardiomyopathy: a case report. Lin HC; Tsai FJ; Shen WC; Tsai CH; Peng CT Acta Paediatr; 2000 Jul; 89(7):880-3. PubMed ID: 10943975 [No Abstract] [Full Text] [Related]
17. Mongolian spots in a sick patient-A diagnosis of infantile GM1 gangliosidosis. Truong K; Fong G; Lewis K; Moghimi A; Prasad A; Hogan P Australas J Dermatol; 2023 Nov; 64(4):553-556. PubMed ID: 37622432 [No Abstract] [Full Text] [Related]
18. Is there a relationship between inborn errors of metabolism and extensive mongolian spots? Mendez HM; Pinto LI; Paskulin GA; Ricachnevsky N Am J Med Genet; 1993 Sep; 47(4):456-7. PubMed ID: 8256803 [TBL] [Abstract][Full Text] [Related]
19. Dermal melanocytosis associated with GM1-gangliosidosis type 1. Bloch LD; Matsumoto FY; Belda W; Giugliani R; Menezes LF; Kim CA; Machado MC Acta Derm Venereol; 2006; 86(2):156-8. PubMed ID: 16648922 [No Abstract] [Full Text] [Related]