RobertNSchimkeMD

Endocrinology • Kansas City, KS

Diabetes, Lipid Metabolism

Physician

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Office
3901 Rainbow Blvd
Dept Of Internal Medicine
Kansas City, KS 66160
Phone+1 913-588-6000
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Summary

Dr. Robert Schimke, MD is an endocrinologist in Kansas City, Kansas. He is currently licensed to practice medicine in Kansas.

Education & Training

University of Kansas School of MedicineResidency, Internal Medicine, 1965 - 1967
University of Kansas School of MedicineInternship, Transitional Year, 1962 - 1963
University of Kansas School of MedicineClass of 1962

Certifications & Licensure

KS State Medical License 1963 - 2016
American Board of Internal Medicine Internal Medicine
American Board of Internal Medicine Endocrinology, Diabetes and Metabolism
American Board of Medical Genetics and Genomics Clinical Genetics

Publications & Presentations

PubMed

41 citations
Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.
Jennifer J. Johnston, Isabelle M. Olivos-Glander, Joyce T. Turner, Kyrieckos A. Aleck, Lynne M. Bird, Lakshmi Mehta, R. Neil Schimke, Heidi A. Heilstedt, J. Edward Spe...> ;American Journal of Medical Genetics. Part A. 2003 Dec 15
2 citations
Regarding cancer predisposition detected by CHG arrays
Debra L. Collins, R. Neil Schimke> ;Genetics in Medicine. 2011 Nov 1
DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors.
Rio Frio, T., Bahubeshi, A., Kanellopoulou, C., Hamel, N., Niedziela, M., Sabbaghian, N., Pouchet, C., Gilbert, L., O'Brien, P. K., Serfas, K., Broderick, P., Houlston...> ;JAMA. 2011 Jan 5
61 citations
Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30-year-old mystery.
R. Neil Schimke, Debra L. Collins, Catherine A. Stolle> ;American Journal of Medical Genetics. Part A. 2010 Jun 1
2 citations
The Hunter-MacDonald syndrome with expanded phenotype including risk of meningioma: an update and review.
Linlea Armstrong, Gail E. Graham, R. Neil Schimke, Debra L. Collins, Daniel J. Kirse, Fiona Costello, Holly H. Ardinger> ;American Journal of Medical Genetics. Part A. 2008 Jan 1
Syndromes with multiple endocrine gland involvement.
Schimke, R. N.> ;Prog Med Genet. 1979
Multiple endocrine adenomatosis syndromes.
Schimke, R. N.> ;Adv Intern Med. 1976
Innovations in human genetics education: College course work in human genetics for elementary, middle, and high school educators in Kansas.
Collins, D. L., Schimke, R. N.> ;Am J Hum Genet. 1988 Apr
An unusual sellar mass--solitary plasmacytoma.
Mandagere, K. A., Schimke, R. N., Kyner, J. L., Bhatia, P. S.> ;Endocr Pract. 1998 Nov 01
HOMOCYSTINURIA. STUDIES OF 20 FAMILIES WITH 38 AFFECTED MEMBERS.
SCHIMKE, R. N., MCKUSICK, V. A., HUANG, T., POLLACK, A. D.> ;JAMA. 1965 Aug 30
Extragonadal germ cell tumors in brothers.
Stany A. D'Silva, Stephan K. Williamson, R. Neil Schimke> ;American Journal of Medical Genetics. 1999 Dec 3
21 citations
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene.
John F. Bradley, Debra L. Collins, R N Schimke, H N Parrott, Paul G. Rothberg> ;American Journal of Medical Genetics. 1999 Nov 19
17 citations
Functioning carotid paraganglioma in the von Hippel-Lindau syndrome.
R N Schimke, Debra L. Collins, Paul G. Rothberg> ;American Journal of Medical Genetics. 1998 Dec 28
16 citations
Congenital nonprogressive myopathy with Möbius and Robin sequence—the Carey-Fineman-Ziter syndrome: A confirmatory report
R N Schimke, Debra L. Collins, J M Hiebert> ;American Journal of Medical Genetics. 1993 Jul 1
Continuation of a case report.
Holmes, G. E., Schimke, R. N., Goertz, K., Mattioli, L., Richardson, W.> ;J Med Genet. 1993 May
Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.
Pegoraro, E., Schimke, R. N., Arahata, K., Hayashi, Y., Stern, H., Marks, H., Glasberg, M. R., Carroll, J. E., Taber, J. W., Wessel, H. B.> ;Am J Hum Genet. 1994 Jun
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei.
Pegoraro, E., Schimke, R. N., Garcia, C., Stern, H., Cadaldini, M., Angelini, C., Barbosa, E., Carroll, J., Marks, W. A., Neville, H. E., Marks, H., Appleton, S., Tori...> ;Neurology. 1995 Apr
Hereditary urogenital adysplasia.
Schimke, R. N., King, C. R.> ;Clin Genet. 1980 Dec
16 citations
Familial joint instability syndrome.
William A. Horton, Debra L. Collins, Arthur A. DeSmet, James Kennedy, R. Neil Schimke, John M. Opitz> ;American Journal of Medical Genetics. 1980 Jan 1
48 citations
Osteopetrosis: Further heterogeneity
William A. Horton, R. Neil Schimke, Tina Iyama> ;The Journal of Pediatrics. 1980 Oct 1
15 citations
Moebius syndrome in a child and extremity defect in her father.
Debra L. Collins, R. Neil Schimke> ;Clinical Genetics. 2008 Apr 23
Pregnancy in a patient with 47,XX,i(Xq) karyotype.
King, C. R., Schimke, R. N.> ;J Med Genet. 1982 Dec
Hyperprolactinemia: the experience at the University of Kansas Medical Center.
Silver, B. J., Schimke, R. N., Kyner, J. L., Lukert, B. P., Bolinger, R. E., Meek, J. C.> ;J Kans Med Soc. 1982 Mar
CT screening of the abdomen in von Hippel-Lindau disease.
Levine, E., Collins, D. L., Horton, W. A., Schimke, R. N.> ;AJR Am J Roentgenol. 1982 Sep
Bezoars. A complication of diabetic gastroparesis.
Silver, B. J., Rhodes, J. B., Schimke, R. N., Greenberger, N. J.> ;J Kans Med Soc. 1983 May
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