MODY--an autosomal dominant type of diabetes. Diagnosis via genetic testing results in better treatment
Karlsson, E.; Groop, L.
Lakartidningen 104(37): 2600-2602
2007
ISSN/ISBN: 0023-7205 PMID: 17970396 Document Number: 608124
Document emailed within 1 workday
Related Documents
Tóth, T.; Nagy, B. 1997: Molecular genetic study of type i autosomal dominant polycystic kidney disease Orvosi Hetilap 138(41): 2638Scherbaum, W.A. 2001: Type 1, type 2 diabetes, MODY and LADA. Making a differential diagnosis MMW Fortschritte der Medizin 143(37): 45-48
Małecki, M.; Krolewski, A.S. 2000: Molecular background and clinical characteristics of autosomal dominant type 2 diabetes mellitus Przeglad lekarski 57 Suppl. 3: 13-18
Milutinovic, J.; Fialkow, P.J.; Phillips, L.A.; Agoda, L.Y.; Bryant, J.I.; Denney, J.D.; Rudd, T.G. 1980: Autosomal dominant polycystic kidney disease: early diagnosis and data for genetic counselling Lancet 1(8180): 1203-1206
Tay, J.S.; Yip, W.C. 1982: Computers in paediatrics. 3. Genetic counselling for autosomal dominant conditions Journal of the Singapore Paediatric Society 24(3-4): 133-137
Karnolski, I.N. 2002: Inherited autosomal dominant polycystic kidney disease--genetic polymorphism Folia Medica 44(4): 7-9
Sessa, A.; Ghiggeri, G.M.; Turco, A.E. 1997: Autosomal dominant polycystic kidney disease: clinical and genetic aspects Journal of Nephrology 10(6): 295-310
Samaan, M.C.; Brennan, A.; Fitzgerald, H.; Roche, E.F.; Hoey, H.M.C.V. 2005: Maturity Onset Diabetes in the Young (MODY) type 3 Irish Medical Journal 98(1): 28-29
Del Vecchio, M.; Cerillo, A.; Ghetti, B.; Amati, A.; Signorelli, C.; Cedrola, G.; Guazzi, G.C. 1971: Genetic study of 2 families (23 subjects) with von Recklinghausen's disease with dominant autosomal heredity Acta Neurologica 26(3): 319-360
Hansen, T.; Urhammer, S.ør.A.; Pedersen, O.B. 2002: Maturity-onset diabetes of the young--MODY. Molecular-genetic, pathophysiological and clinical characteristics Ugeskrift for Laeger 164(15): 2017-2022
Zhang, W-li.; Mei, C-lin. 2006: Genetic heterogeneity and phenotypes of autosomal dominant polycystic kidney disease in Chinese Han nationality Zhonghua Yi Xue Za Zhi 86(22): 1516-1521
Idris, M.N.; Sokrab, T.O. 2002: Autosomal dominant cerebellar ataxia type 1 in a Sudanese family Neurosciences 7(2): 83-85
Vezzoli, G.; Arcidiacono, T.; Paloschi, V.; Terranegra, A.; Biasion, R.; Weber, G.; Mora, S.; Syren, M.Louise.; Coviello, D.; Cusi, D.; Bianchi, G.; Soldati, L. 2006: Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome Journal of Nephrology 19(4): 525-528
Lebedev, N.B.; Shcherbacheva, L.N.; Koledova, E.B.; Trofilmenko, E.V.; Maĭorov, A.I. 1994: Non-insulin-dependent diabetes mellitus in young patients with autosomal dominant inheritance Problemy Endokrinologii 40(1): 9-14
Martello, C.; Stangoni, G.; Mezzetti, D.; Calabro, A.; Cianfrini, D.; Lungarotti, M.S. 1992: Spondylo-costal dysostosis: presentation of a new case with autosomal dominant heredity and discussion of problems in genetic counseling La Pediatria Medica e Chirurgica: Medical and Surgical Pediatrics 14(4): 465-468
López-Corona, E.; García-González, V.M.; Gabilondo, F. 2004: Results of nephrectomy in patients with autosomal dominant polycystic kidney disease Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 56(4): 437-442
Knoblauch, H.; Urban, M.; Tinschert, S. 1999: Autosomal recessive versus autosomal dominant inheritance in Larsen syndrome: report of two affected sisters Genetic Counseling 10(3): 315-320
De Arriba de la Fuente, G.; García Martín, F.; Sánchez Ortega, F.; Sánchez Heras, M.; Parra Cid, T.; Blanco Santos, A.; Jarillo Ibáñez, M.D. 1995: Autosomal dominant polycystic kidney disease. a comparative genetic and clinico-radiological study between patients with normal renal function and their healthy relatives Revista Clinica Espanola 195(9): 600-607
Hofbauer, M.; Schnyder, U.W. 1974: Differential diagnosis of autosomal-dominant chthyosis vulgaris and X-chromosome ichthyosis Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 25(7): 319-325
Jeerathanyasakun, Y.; Sukswai, P. 2003: Bilateral asynchronous humeral shaft fractures in a patient with autosomal dominant osteopetrosis type Ii (Albers-Schonberg disease) Journal of the Medical Association of Thailand 86(Suppl 3): S667-S672