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3. Autosomal dominant insulin resistance syndrome due to postbinding defect. Seemanová E; Rüdiger HW; Dreyer M Am J Med Genet; 1992 Dec; 44(6):705-12. PubMed ID: 1282780 [TBL] [Abstract][Full Text] [Related]
4. Ophthalmologic and systemic features of the Alström syndrome: report of 9 cases. Van den Abeele K; Craen M; Schuil J; Meire FM Bull Soc Belge Ophtalmol; 2001; (281):67-72. PubMed ID: 11702646 [TBL] [Abstract][Full Text] [Related]
5. Pigmentary retinopathy, hearing loss, mental retardation, and dysmorphism in sibs: a new syndrome? Hersh JH; Podruch PE; Weisskopf B Birth Defects Orig Artic Ser; 1982; 18(3B):175-82. PubMed ID: 7139098 [No Abstract] [Full Text] [Related]
6. Familial hyperinsulinaemia associated with epilepsy and mental retardation--a syndrome of familial insulin resistance. Idris I; Miller D; Page SR Diabet Med; 2004 Jun; 21(6):628-31. PubMed ID: 15154952 [TBL] [Abstract][Full Text] [Related]
7. A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance. Edwards JA; Sethi PK; Scoma AJ; Bannerman RM; Frohman LA Am J Med; 1976 Jan; 60(1):23-32. PubMed ID: 1251844 [TBL] [Abstract][Full Text] [Related]
8. [Insulin resistance: from clinical diagnosis to molecular genetics. Implications in diabetes mellitus]. Jaffiol C; Rouard M; Macari F; Lautier C; Ait el Mkadem S; Méchaly I; Brun JF; Renard E; Cros G; Bringer J; Grigorescu F Bull Acad Natl Med; 1999; 183(9):1761-75; discussion 1775-7. PubMed ID: 10987057 [TBL] [Abstract][Full Text] [Related]
9. Woodhouse-Sakati syndrome: case report and symptoms review. Medica I; Sepcić J; Peterlin B Genet Couns; 2007; 18(2):227-31. PubMed ID: 17710875 [TBL] [Abstract][Full Text] [Related]
10. Rabson-Mendenhall syndrome. Parveen BA; Sindhuja R Int J Dermatol; 2008 Aug; 47(8):839-41. PubMed ID: 18717867 [TBL] [Abstract][Full Text] [Related]
11. Hepatic dysfunction in Alström disease. Connolly MB; Jan JE; Couch RM; Wong LT; Dimmick JE; Rigg JM Am J Med Genet; 1991 Sep; 40(4):421-4. PubMed ID: 1746604 [TBL] [Abstract][Full Text] [Related]
13. Usher syndrome in four siblings from a consanguineous family of Pakistani origin. Trop I; Schloss MD; Polomeno R; Der Kaloustian V J Otolaryngol; 1995 Apr; 24(2):102-4. PubMed ID: 7602669 [TBL] [Abstract][Full Text] [Related]
15. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism. Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066 [TBL] [Abstract][Full Text] [Related]
16. Morfan: a new syndrome characterized by mental retardation, pre- and postnatal overgrowth, remarkable face and acanthosis nigricans in 5-year-old boy. Seemanová E; Rüdiger HW; Dreyer M Am J Med Genet; 1993 Feb; 45(4):525-8. PubMed ID: 8465862 [No Abstract] [Full Text] [Related]
17. Insulin resistance with acanthosis nigricans and acral hypertrophy. Holdaway IM; Frengley PA; Graham FM; Wong M N Z Med J; 1984 May; 97(755):286-8. PubMed ID: 6587221 [TBL] [Abstract][Full Text] [Related]
18. [A case of insulin receptor abnormality (type A)]. Kamada T; Horinosono M; Nishi M; Setoyama M; Oki T; Nagata Y; Arima T; Tashiro M; Otsuji S Igaku Kenkyu; 1992 Feb; 62(1):25-9. PubMed ID: 1523941 [TBL] [Abstract][Full Text] [Related]
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20. Three new cases of Alström syndrome. Benso C; Hadjadj E; Conrath J; Denis D Graefes Arch Clin Exp Ophthalmol; 2002 Aug; 240(8):622-7. PubMed ID: 12192455 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]