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23. Coats' disease: occurrence in a four-month-old infant. Dow DS South Med J; 1973 Jul; 66(7):836-8. PubMed ID: 4752234 [No Abstract] [Full Text] [Related]
24. Glaucomatous cupping of the optic disc in the young. Shaffer RN Trans Ophthalmol Soc N Z; 1973; 25():77-80. PubMed ID: 4519235 [No Abstract] [Full Text] [Related]
25. A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy. Doğancı T; Yüksel Konuk BE; Alpan N; Konuk O; Hämäläinen RH; Lehesjoki AE; Tekin M Clin Dysmorphol; 2007 Jul; 16(3):173-176. PubMed ID: 17551331 [TBL] [Abstract][Full Text] [Related]
26. [Dysendocrine nanism]. Romano C Minerva Pediatr; 1966 Oct; 18(30):1791-802. PubMed ID: 5995745 [No Abstract] [Full Text] [Related]
27. 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]
28. Funduscopic and angiographic appearance in the neuronal ceroid lipofuscinoses. Hainsworth DP; Liu GT; Hamm CW; Katz ML Retina; 2009 May; 29(5):657-68. PubMed ID: 19289983 [TBL] [Abstract][Full Text] [Related]
29. Mulibrey heart disease: clinical manifestations, long-term course, and results of pericardiectomy in a series of 49 patients born before 1985. Lipsanen-Nyman M; Perheentupa J; Rapola J; Sovijärvi A; Kupari M Circulation; 2003 Jun; 107(22):2810-5. PubMed ID: 12756154 [TBL] [Abstract][Full Text] [Related]
30. Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome. Majewski F; Goecke T Am J Med Genet; 1982 May; 12(1):7-21. PubMed ID: 7046443 [No Abstract] [Full Text] [Related]
31. The ocular manifestations of Weissenbacher-Zweymuller syndrome. Rabinowitz R; Gradstein L; Galil A; Levy J; Lifshitz T Eye (Lond); 2004 Dec; 18(12):1258-63. PubMed ID: 15044941 [TBL] [Abstract][Full Text] [Related]
33. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy. Tyni T; Kivelä T; Lappi M; Summanen P; Nikoskelainen E; Pihko H Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380 [TBL] [Abstract][Full Text] [Related]
34. [Recurring congenital intraocular toxoplasmosis with peripheral choroid coloboma]. Röchling U Ber Zusammenkunft Dtsch Ophthalmol Ges; 1969; 69():162-5. PubMed ID: 4982264 [No Abstract] [Full Text] [Related]
35. [Clinical observations of embryonal seam of the choroid]. Novokhatskiĭ AS; Serdiuchenko VI Oftalmol Zh; 1974; 29(8):580-3. PubMed ID: 4453393 [No Abstract] [Full Text] [Related]
36. [What should we think about morning glory syndromes?]. Amalric P Bull Soc Ophtalmol Fr; 1982; 82(6-7):793-9. PubMed ID: 7172374 [No Abstract] [Full Text] [Related]
37. Mulibrey-nanism: dwarfism with muscle, liver, brain and eye involvement. Perheentupa J; Autio S; Leisti S; Raitta C Acta Paediatr Scand Suppl; 1970; 206():Suppl 206:74+. PubMed ID: 5277003 [No Abstract] [Full Text] [Related]
38. [Idiopathic central serous chorioretinopathy]. Binaghi M; Prevost Y; Coscas G J Fr Ophtalmol; 1984; 7(5):419-36. PubMed ID: 6389656 [No Abstract] [Full Text] [Related]
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