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.
242 related articles for article (PubMed ID: 19624984)
1. Heterogeneity and atypical presentation in infantile systemic hyalinosis with severe labio-gingival enlargement: first Egyptian report. El-Kamah GY; Mostafa MI Dermatol Online J; 2009 May; 15(5):6. PubMed ID: 19624984 [TBL] [Abstract][Full Text] [Related]
2. A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis. Büyükgebiz B; Oztürk Y; Arslan N; Ozer E Turk J Pediatr; 2003; 45(3):258-60. PubMed ID: 14696808 [TBL] [Abstract][Full Text] [Related]
3. Infantile systemic hyalinosis: Case report and review of the literature. Lindvall LE; Kormeili T; Chen E; Ramirez MC; Grum-Tokars V; Glucksman MJ; Martignetti JA; Zaragoza MV; Dyson SW J Am Acad Dermatol; 2008 Feb; 58(2):303-7. PubMed ID: 18222328 [TBL] [Abstract][Full Text] [Related]
10. Infantile systemic hyalinosis: report of four cases of a disease, fatal in infancy, apparently different from juvenile systemic hyalinosis. Landing BH; Nadorra R Pediatr Pathol; 1986; 6(1):55-79. PubMed ID: 2434938 [TBL] [Abstract][Full Text] [Related]
11. Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis-A Case Report. Krasuska-Sławińska E; Polnik D; Rokicki D; Koeber B J Oral Maxillofac Surg; 2015 Oct; 73(10):1962.e1-5. PubMed ID: 26207694 [TBL] [Abstract][Full Text] [Related]
17. Infantile systemic hyalinosis: report of three Iranian children and review of the literature. Aghighi Y; Bahremand S; Nematollahi LR Clin Rheumatol; 2007 Jan; 26(1):128-30. PubMed ID: 16328093 [TBL] [Abstract][Full Text] [Related]
18. Juvenile hyaline fibromatosis and infantile systemic hyalinosis overlap associated with a novel mutation in capillary morphogenesis protein-2 gene. Antaya RJ; Cajaiba MM; Madri J; Lopez MA; Ramirez MC; Martignetti JA; Reyes-Múgica M Am J Dermatopathol; 2007 Feb; 29(1):99-103. PubMed ID: 17284973 [TBL] [Abstract][Full Text] [Related]
19. Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2). Shieh JT; Swidler P; Martignetti JA; Ramirez MC; Balboni I; Kaplan J; Kennedy J; Abdul-Rahman O; Enns GM; Sandborg C; Slavotinek A; Hoyme HE Pediatrics; 2006 Nov; 118(5):e1485-92. PubMed ID: 17043134 [TBL] [Abstract][Full Text] [Related]
20. Intestinal lymphangiectasia in a patient with infantile systemic hyalinosis syndrome: a rare cause of protein-losing enteropathy. Alreheili K; AlMehaidib A; Alsaleem K; Banemi M; Aldekhail W; Al-Mayouf SM Ann Saudi Med; 2012; 32(2):206-8. PubMed ID: 22366835 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]