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.
24. Report of two Syrian siblings with Mulibrey nanism. Al Saadi T; Alkhatib M; Turk T; Turkmani K; Abbas F; Khouri L Oxf Med Case Reports; 2015 Dec; 2015(12):367-70. PubMed ID: 26664725 [TBL] [Abstract][Full Text] [Related]
25. [Certain neuroendocrine factors of regulation in children with somatogenic and hypophyseal nanism]. Ozerova MR; Osinskaia VO; Kurbanov T; Anishchuk VP; Markova IS Pediatriia; 1975 Jul; (7):16-9. PubMed ID: 1215082 [No Abstract] [Full Text] [Related]
26. [Mulibrey nanism in a Mexican child]. Sánchez-Corona J; Morán-Vázquez O; Rivera H; Hernández A; Serrano-Lucas JI; Ocampo-Campos R; Lasso-Avalos L; María-Cantú J Bol Med Hosp Infant Mex; 1983 Jan; 40(1):45-8. PubMed ID: 6830647 [No Abstract] [Full Text] [Related]
27. Thoracoscopic pericardiectomy for constrictive pericarditis in a pediatric patient with mulibrey nanism. Christov G; Burch M; Andrews R; Hurst J; Ashworth M; Mustafa M; Muthialu N World J Pediatr Congenit Heart Surg; 2013 Oct; 4(4):442-3. PubMed ID: 24327644 [TBL] [Abstract][Full Text] [Related]
28. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism. Avela K; Lipsanen-Nyman M; Idänheimo N; Seemanová E; Rosengren S; Mäkelä TP; Perheentupa J; Chapelle AD; Lehesjoki AE Nat Genet; 2000 Jul; 25(3):298-301. PubMed ID: 10888877 [TBL] [Abstract][Full Text] [Related]
29. Where genetics and pathology meet: mulibrey nanism. Hes FJ; Morreau H J Pathol; 2009 Jun; 218(2):143-5. PubMed ID: 19347900 [TBL] [Abstract][Full Text] [Related]
34. Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease. Baumgartner MR; Verhoeven NM; Jakobs C; Roels F; Espeel M; Martinez M; Rabier D; Wanders RJ; Saudubray JM Neurology; 1998 Nov; 51(5):1427-32. PubMed ID: 9818873 [TBL] [Abstract][Full Text] [Related]
35. Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction. Perheentupa J; Autio S; Leisti S; Raitta C; Tuuteri L Lancet; 1973 Aug; 2(7825):351-5. PubMed ID: 4124529 [No Abstract] [Full Text] [Related]
36. [Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers]. Molzer B; Stöckler S; Bernheimer H Wien Klin Wochenschr; 1992; 104(21):665-70. PubMed ID: 1282286 [TBL] [Abstract][Full Text] [Related]
37. [Etiopathogenetic aspects of the so-called non-endocrine infantile nanism]. Lodi A; Ravaglia G; Ferramosca B; Pacetti P Minerva Med; 1973 Jul; 64(56):2940-1. PubMed ID: 4742631 [No Abstract] [Full Text] [Related]
38. Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teeth. Clayton-Smith J; Krajewska-Walasek M; Fryer A; Donnai D Clin Dysmorphol; 1994 Apr; 3(2):115-20. PubMed ID: 8055130 [TBL] [Abstract][Full Text] [Related]
39. The peroxisome: nervous system role of a previously underrated organelle. The 1987 Robert Wartenberg lecture. Moser HW Neurology; 1988 Oct; 38(10):1617-27. PubMed ID: 2458548 [No Abstract] [Full Text] [Related]