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5. Prenatal analysis of the insulin receptor gene in a family with leprechaunism. Longo N; Langley SD; Still MJ; Elsas LJ Prenat Diagn; 1995 Nov; 15(11):1070-4. PubMed ID: 8606887 [TBL] [Abstract][Full Text] [Related]
6. Two mutations in the insulin receptor gene of a patient with leprechaunism: application to prenatal diagnosis. Longo N; Langley SD; Griffin LD; Elsas LJ J Clin Endocrinol Metab; 1995 May; 80(5):1496-501. PubMed ID: 7538143 [TBL] [Abstract][Full Text] [Related]
7. [Leprechaunism: an inherited insulin resistance syndrome caused by the defect of insulin receptor]. Jiang L; Liu C; Wang WQ; Ye L; Zhu N; Zhou WW; Su TW; Li XY; Ning G Zhonghua Nei Ke Za Zhi; 2006 Sep; 45(9):730-3. PubMed ID: 17166446 [TBL] [Abstract][Full Text] [Related]
8. Molecular defects in the insulin receptor in patients with leprechaunism and in their parents. Reddy SS; Muller-Wieland D; Kriauciunas K; Kahn CR J Lab Clin Med; 1989 Aug; 114(2):165-70. PubMed ID: 2569023 [TBL] [Abstract][Full Text] [Related]
9. A homozygous kinase-defective mutation in the insulin receptor gene in a patient with leprechaunism. Takahashi Y; Kadowaki H; Momomura K; Fukushima Y; Orban T; Okai T; Taketani Y; Akanuma Y; Yazaki Y; Kadowaki T Diabetologia; 1997 Apr; 40(4):412-20. PubMed ID: 9112018 [TBL] [Abstract][Full Text] [Related]
10. Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndrome. Gastier JM; Berg MA; Vesterhus P; Reiter EO; Francke U Hum Mutat; 2000 Oct; 16(4):323-33. PubMed ID: 11013443 [TBL] [Abstract][Full Text] [Related]
11. [Leprechaunism caused by mutations in the insulin receptor gene]. Murashita M; Tajima T; Nakae J; Fujieda K Nihon Rinsho; 2002 Feb; 60(2):344-9. PubMed ID: 11857924 [TBL] [Abstract][Full Text] [Related]
13. Identification of two novel insulin receptor mutations, Asp59Gly and Leu62Pro, in type A syndrome of extreme insulin resistance. Rouard M; Macari F; Bouix O; Lautier C; Brun JF; Lefebvre P; Renard E; Bringer J; Jaffiol C; Grigorescu F Biochem Biophys Res Commun; 1997 May; 234(3):764-8. PubMed ID: 9175790 [TBL] [Abstract][Full Text] [Related]
14. Comparison of the insulin receptor gene and insulin binding in families with severe insulin resistance. Elsas LJ; Longo N; Fotion TR; Langley S Trans Assoc Am Physicians; 1988; 101():137-48. PubMed ID: 2908370 [No Abstract] [Full Text] [Related]
15. Dental and craniofacial characteristics in a patient with leprechaunism treated with insulin-like growth factor-I. Fukunaga T; Murakami T; Tanaka H; Miyawaki S; Yamashiro T; Takano-Yamamoto T Angle Orthod; 2008 Jul; 78(4):745-51. PubMed ID: 18302477 [TBL] [Abstract][Full Text] [Related]
16. Homozygosity for a null allele of the insulin receptor gene in a patient with leprechaunism. Hone J; Accili D; Psiachou H; Alghband-Zadeh J; Mitton S; Wertheimer E; Sinclair L; Taylor SI Hum Mutat; 1995; 6(1):17-22. PubMed ID: 7550226 [TBL] [Abstract][Full Text] [Related]
18. Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. Campbell C; Cucci RA; Prasad S; Green GE; Edeal JB; Galer CE; Karniski LP; Sheffield VC; Smith RJ Hum Mutat; 2001 May; 17(5):403-11. PubMed ID: 11317356 [TBL] [Abstract][Full Text] [Related]
19. Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptor. Desbois-Mouthon C; Danan C; Amselem S; Blivet-Van Eggelpoel MJ; Sert-Langeron C; Goossens M; Besmond C; Capeau J; Caron M Metabolism; 1996 Dec; 45(12):1493-500. PubMed ID: 8969282 [TBL] [Abstract][Full Text] [Related]
20. Deletion of exon 3 of the insulin receptor gene in a kindred with a familial form of insulin resistance. Wertheimer E; Litvin Y; Ebstein RP; Bennet ER; Barbetti F; Accili D; Taylor SI J Clin Endocrinol Metab; 1994 May; 78(5):1153-8. PubMed ID: 8175972 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]