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Results: 1-14 |
Results: 14
DIABETES-ASSOCIATED DELETION IN MITOCHONDRIAL-DNA IN A PATIENT WITH PEARSONS PANCREAS BONE-MARROW SYNDROME
Authors: VANDENOUWELAND JMW BRUINING GJ MAASSEN JA
Citation: Jmw. Vandenouweland et al., DIABETES-ASSOCIATED DELETION IN MITOCHONDRIAL-DNA IN A PATIENT WITH PEARSONS PANCREAS BONE-MARROW SYNDROME, Diabetologia, 41, 1998, pp. 404-404
HETEROPLASMY OF THE MITOCHONDRIAL A3243G MUTATION AND THE PHENOTYPE OF MATERNALLY INHERITED DIABETES AND DEAFNESS
Authors: VANESSEN EHR THART LM JANSEN JJ VANDENOUWELAND JMW MAASSEN JA LEMKES HHPJ
Citation: Ehr. Vanessen et al., HETEROPLASMY OF THE MITOCHONDRIAL A3243G MUTATION AND THE PHENOTYPE OF MATERNALLY INHERITED DIABETES AND DEAFNESS, Diabetologia, 41, 1998, pp. 433-433
MUTATION IN MITOCHONDRIAL TRNA(LEU(UUR)) GENE ASSOCIATED WITH PROGRESSIVE KIDNEY-DISEASE
Authors: JANSEN JJ MAASSEN JA VANDERWOUDE FJ LEMMINK HAJ VANDENOUWELAND JMW THART LM SMEETS HJM BRUIJN JA LEMKES HHPJ
Citation: Jj. Jansen et al., MUTATION IN MITOCHONDRIAL TRNA(LEU(UUR)) GENE ASSOCIATED WITH PROGRESSIVE KIDNEY-DISEASE, Journal of the American Society of Nephrology, 8(7), 1997, pp. 1118-1124
DETECTION OF MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN FIBROBLASTS OFPATIENTS WITH PEARSONS-SYNDROME BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: VANDECORPUT MPC VANDENOUWELAND JMW DIRKS RW THART LM BRUINING GJ MAASSEN JA RAAP AK
Citation: Mpc. Vandecorput et al., DETECTION OF MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN FIBROBLASTS OFPATIENTS WITH PEARSONS-SYNDROME BY 2-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION, The Journal of histochemistry and cytochemistry, 45(1), 1997, pp. 55-61
MATERNALLY INHERITED DIABETES AND DEAFNESS - A DIABETIC SUBTYPE ASSOCIATED WITH A MUTATION IN MITOCHONDRIAL-DNA
Authors: MAASSEN JA VANDENOUWELAND JMW THART LM LEMKES HHPJ
Citation: Ja. Maassen et al., MATERNALLY INHERITED DIABETES AND DEAFNESS - A DIABETIC SUBTYPE ASSOCIATED WITH A MUTATION IN MITOCHONDRIAL-DNA, Hormone and Metabolic Research, 29(2), 1997, pp. 50-55
THE MOLECULAR-BASIS AND CLINICAL CHARACTERISTICS OF MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD), A RECENTLY RECOGNIZED DIABETIC SUBTYPE
Authors: MAASSEN JA JANSEN JJ KADOWAKI T VANDENOUWELAND JMW THART LM LEMKES HHPJ
Citation: Ja. Maassen et al., THE MOLECULAR-BASIS AND CLINICAL CHARACTERISTICS OF MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD), A RECENTLY RECOGNIZED DIABETIC SUBTYPE, EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 104(3), 1996, pp. 205-211
MITOCHONDRIAL DIABETES-MELLITUS - A REVIEW
Authors: GERBITZ KD VANDENOUWELAND JMW MAASSEN JA JAKSCH M
Citation: Kd. Gerbitz et al., MITOCHONDRIAL DIABETES-MELLITUS - A REVIEW, Biochimica et biophysica acta. Molecular basis of disease, 1271(1), 1995, pp. 253-260
MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD) - A DISTINCT SUBTYPE OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL TRNA(LEU(UUR)) GENE POINT MUTATION
Authors: VANDENOUWELAND JMW LEMKES HHPJ GERBITZ KD MAASSEN JA
Citation: Jmw. Vandenouweland et al., MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD) - A DISTINCT SUBTYPE OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL TRNA(LEU(UUR)) GENE POINT MUTATION, Muscle & nerve, 1995, pp. 124-130
NATURAL COURSE OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS)
Authors: RASKER SP JANSEN JJ VANDENOUWELAND JMW THART LM MAASSSEN JA LEMKES HHPJ
Citation: Sp. Rasker et al., NATURAL COURSE OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS), Diabetologia, 38, 1995, pp. 78-78
MUTATION IN MITOCHONDRIAL TRANSFER-RNA(LEU(UUR)) GENE ASSOCIATED WITHDIABETES AND SEVERE NONDIABETIC KIDNEY-DISEASE
Authors: LEMKES HHPJ JANSEN JJ VANDENOUWELAND JMW VANDERWOUDE FJ THART LM BRUYN JA MAASSEN JA
Citation: Hhpj. Lemkes et al., MUTATION IN MITOCHONDRIAL TRANSFER-RNA(LEU(UUR)) GENE ASSOCIATED WITHDIABETES AND SEVERE NONDIABETIC KIDNEY-DISEASE, Diabetologia, 38, 1995, pp. 229-229
CLINICAL PRESENTATION OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS)
Authors: LEMKES HHPJ JANSEN NJ RASKER SP THART LM VANDENOUWELAND JMW MAASSEN TA
Citation: Hhpj. Lemkes et al., CLINICAL PRESENTATION OF MIDD (MATERNALLY INHERITED DIABETES AND DEAFNESS), Diabetes, 44, 1995, pp. 233-233
PREVALENCE OF MATERNALLY INHERITED DIABETES AND DEAFNESS IN DIABETIC POPULATIONS IN THE NETHERLANDS
Authors: THART LM LEMKES HHPJ HEINE RJ STOLK RP FESKENS EJM JANSEN JJ VANDERDOES FEE GROBBEE DE KROMHOUT D VANDENOUWELAND JMW MAASSEN JA
Citation: Lm. Thart et al., PREVALENCE OF MATERNALLY INHERITED DIABETES AND DEAFNESS IN DIABETIC POPULATIONS IN THE NETHERLANDS, Diabetologia, 37(11), 1994, pp. 1169-1170
MATERNALLY INHERITED DIABETES AND DEAFNESS IS A DISTINCT SUBTYPE OF DIABETES AND ASSOCIATES WITH A SINGLE-POINT MUTATION IN THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE
Authors: VANDENOUWELAND JMW LEMKES HHPJ TREMBATH RC ROSS R VELHO G COHEN D FROGUEL P MAASSEN JA
Citation: Jmw. Vandenouweland et al., MATERNALLY INHERITED DIABETES AND DEAFNESS IS A DISTINCT SUBTYPE OF DIABETES AND ASSOCIATES WITH A SINGLE-POINT MUTATION IN THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE, Diabetes, 43(6), 1994, pp. 746-751
MATERNALLY INHERITED TYPE-II DIABETES-MELLITUS AND DEAFNESS IS ASSOCIATED WITH A MITOCHONDRIAL-DNA POINT MUTATION
Authors: VANDENOUWELAND JMW LEMKES HHPJ MAASSEN JA
Citation: Jmw. Vandenouweland et al., MATERNALLY INHERITED TYPE-II DIABETES-MELLITUS AND DEAFNESS IS ASSOCIATED WITH A MITOCHONDRIAL-DNA POINT MUTATION, Diabetologia, 36, 1993, pp. 10000003-10000003
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