A LARGE FAMILY WITH CHARCOT-MARIE-TOOTH TYPE 1A AND TYPE 2 DIABETES MELLITUS

REFERENCES

• Auer-Grumbach M., Wagner K., Strasser-Fuchs S., Loscher W. N., Fazekas F., Millner M., Hartung H. P., Nicholson G. A. Clinical predominance of proximal upper limb weakness in CMT1A syndrome. Muscle & Nerve 2000; 23(8)1243–1249, [CSA]
   PubMedGoogle Scholar
• Berciano J., Garcia A., Combarros O. Initial semeiology in children with Charcot-Marie-Tooth disease 1A duplication. Muscle & Nerve 2003; 27(1)34–39, [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Çelik M., Forta H., Parman Y., Bissar- Tadmourit N., Demirkiran K., Battaloglu E. Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus. Diabetic Medicine 2001; 18(8)685–686, [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Dematteis M., Pepin J. L., Jeanmart M., Deschaux C., Labarre-Vila A., Levy P. Charcot-Marie-Tooth disease and sleep apnoea syndrome: A family study. Lancet 2001; 357(9252)267–272, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Dyck P. J., Chance P., Lebo R., Carney J. A. Hereditary motor and sensory neuropathies. Peripheral neuropathy, 3rd ed., P. J. Dyck, P. K. Thomas, J. W. Griffin, et al. WB Saunders, Philadelphia 1993; 1094–1136
   Google Scholar
• Fajans S. S., Bell G. I., Polonsky K. S. Molecular mechanism and clinical pathophysiology of maturityonset diabetes of young. New England Journal of Medicine 2001; 345(13)971–980, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Gokcel A., Baltali M., Tarim E., Bagis T., Gümürdülü Y., Karakose H., Yalcin F., Akbaba M., Guvener N. Detection of insulin resistance in Turkish adults: A hospital-based study. Diabetes Obesity and Metabolism 2003; 5(2)126–130, [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Hoogendijk J. E., Hensels G. W., Gabreels-Festen A. A., Gabreels F. J., Janssen E. A., de Jonghe P., Martin J. J., van Broeckhoven C., Valentijn L. J., Baas F. De-novo mutation in hereditary motor and sensory neuropathy type I. Lancet 1992; 339(8801)1081–1082, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Kahn C. R. Insulin action, diabetogenes and the causes of type two diabetes. Diabetes 1994; 43(8)1066–1084, [PUBMED], [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Kalm C. R., Vicent D., Doria A. Genetics of non- insulin-dependent (type 2) diabetes mellitus. Annual Review of Medicine 1996; 47: 507–531, [CSA]
   Google Scholar
• Kovach M. J., Campbell K. C., Herman K., Waggoner B., Gelber D., Hughes L. F., Kimonis V. E. Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: Delineation of the clinical features and review of the literature. American Journal Medical Genetics 2002; 108(4)295–303, [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Latour P., Boutrand L., Levy N., Bernard R., Boyer A., Claustrat F., Chazot G., Boucherat M., Vandenberg A. Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplication. Clinical Chemistry 2001; 47(5)829–837, [PUBMED], [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Lupski J. R., de Oca-Luna R. M., Slaugenhaupt S., Pentao L., Guzzetta V., Trask B. J., Saucedo-Cardenas O., Barker D. F., Killian J. M., Garcia C. A. DNA Duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 1991; 66(2) 219–232, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Lupski J. R., Wise C. A., Kuwano A., Pentao L., Parke J. T., Glaze D. G., Ledbetter D. H., Greenberg F., Patel P. I. Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A. Nature Genetics 1992; 1(1)29–33, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Lupski J. R., Pentao L., Williams L. L., Patel P. I. Stable inheritance of the CMT1A DNA duplication in two patients with CMT1 and NF1. American Journal Medical Genetic 1993; 45(1)92–96, [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Mostacciuolo M. L., Schiavon F., Angelini C., Miccoli B., Piccolo F., Danieli G. A. Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1. Neuroepidemiology 1995; 14(2) 49–53, [PUBMED], [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Pareyson D. Charcot-Marie-Tooth Disease and related neuropathies: Molecular basis for distintion and diagnosis. Muscle & Nerve 1999; 22(11)1498–1509, [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Rabasa-Lhoret R., Bastard J. P., Jan V., Ducluzeau P. H., Andreelli F., Guebre F. Modified Quantitative Insulin Sensitivity Check index is beter correlated to hyperinsulinemic glucose clamp than other fasting-based index of insulin sensitivity in different insulin-resistant states. Journal of Clinical Endocrinology and Metabolism 2003; 88(10)4917–4923, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Stern M. P. The search for type 2 diabetes susceptibility genes using whole-genome scans: An epidemiolologist's perpective. Diabetes Metabolism Research and Reviews 2002; 18(2)106–113, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• The DECODE study group on behalf of the European Diabetes Epidemiology group. Glucose tolerance and mortality: Comparison of WHO and American Diabetes Association diagnostic criteria. The DECODE study group. European Diabetes Epidemiology Group. Diabetes epidemiology: Collaborative analysis of diagnostic criteria in Europe. Lancet 1999; 354(9179) 617–621, [CSA], [CROSSREF]
   PubMedGoogle Scholar
• The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care 1997; 20(7) 1183–1197, [CSA]
   PubMed Web of Science ®Google Scholar
• Thomas P. K., Marques W, Jr., Davis M. B., Sweeney M. G., King R. H., Bradley J. L., Muddle J. R., Tyson J., Malcolm S., Harding A. E. The phenotypic manifestations of chromosome 17p11.2 duplication. Brain 1997; 120(Pt 3)463–478, [CSA]
   Google Scholar
• Valentijn L. J., Baas F., Wolterman R. A., Hoogendijk van den J. E., Bosch N. H., Zorn I., Gabreels-Festen A. W., de Visser M., Bolhuis P. A. Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A. Nature Genetics 1992; 2(4)288–291, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Valentijn L. J., Bolhuis P. A., Zorn I., Hoogendijk van den J. E., Bosch N., Hensels G. W., Stanton V. P., Jr. Housman D. E., Fischbeck K. H., Ross D. A. The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A. Nature Genetics 1992; 1(3)166–170, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Vance J. M. Many faces of Charcot-Marie-Tooth Disease. Archives of Neurology 2000; 57(5)638–640, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Velho G., Robert J. J. Maturity-onset diabetes of the young (MODY): Genetic and clinical characteristics. Hormone Research 2002; 57(Suppl 1)29–33, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar