Physician
Endocrinology
Dr. Robert N. Schimke, MD
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Dr. Robert N. Schimke is an expert in the field of Endocrinology. He attended University of Kansas School of Medicine. Dr. Robert N. Schimke is a published physician. He published 100 publications, including: 'Functioning carotid paraganglioma in the von Hippel-Lindau syndrome.'
Publications
- Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome.
- Regarding Cancer predisposition detected by CHG arrays.
- DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors.
- Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30-year-old mystery.
- The Hunter-MacDonald syndrome with expanded phenotype including risk of meningioma: an update and review.
- Syndromes with multiple endocrine gland involvement.
- Multiple endocrine adenomatosis syndromes.
- Innovations in human genetics education: College course work in human genetics for elementary, middle, and high school educators in Kansas.
- An unusual sellar mass--solitary plasmacytoma.
- HOMOCYSTINURIA. STUDIES OF 20 FAMILIES WITH 38 AFFECTED MEMBERS.
- Extragonadal germ cell tumors in brothers.
- Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene.
- Functioning carotid paraganglioma in the von Hippel-Lindau syndrome.
- Congenital nonprogressive myopathy with Möbius and Robin sequence--the Carey-Fineman-Ziter syndrome: a confirmatory report.
- Continuation of a case report.
- Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.
- Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei.
- Hereditary urogenital adysplasia.
- Familial joint instability syndrome.
- Osteopetrosis: further heterogeneity.
- Moebius syndrome in a child and extremity defect in her father.
- Pregnancy in a patient with 47,XX,i(Xq) karyotype.
- Hyperprolactinemia: the experience at the University of Kansas Medical Center.
- CT screening of the abdomen in von Hippel-Lindau disease.
- Bezoars. A complication of diabetic gastroparesis.
- Familial extragonadal germ cell tumors.
- Choriocarcinoma, thyrotoxicosis, and the Klinefelter syndrome.
- A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness.
- Immunoregulation Abnormalities in familial Addison's disease.
- Genetic counseling. The physician's experience.
- Genetic aspects of multiple endocrine neoplasia.
- Case reports; Cimetidine in the management of synchronous crises of MEA I.
- Calcinosis, Raynaud''s phenomenon, sclerodactyly, and telangiectasia. The CRST syndrome.
- Upper-limb cardiovascular syndrome. A family study.
- Homocystinuria simulating the Marfan syndrome.
- Schizophrenia in a patient with a defect in methionine metabolism.
- Familial amyloid-producing medullary Thyroid carcinoma and pheochromocytoma. A distinct genetic entity.
- Genetic Abnormalities in endocrine function.
- The "pink spot" in schizophrenics and its absence in homocystinurics.
- Low methionine diet treatment of homocystinuria.
- Drugs and heredity. Pharmacogenetics--the study of heritable variations in drug response.
- Hereditary renal-retinal dysplasia.
- Craniosynostosis-syndactylism.
- Hereditary cup-shaped ears and the Pierre Robin syndrome.
- Hypogammaglobulinemia with nodular lymphoid hyperplasia of the small bowel.
- Roussy-Lévy syndrome: report of a kindred and discussion of the nosology.
- [The campomelic syndrome].
- The hereditary nephritides.
- Chronic mucocutaneous moniliasis with impaired delayed hypersensitivity.
- The Kallmann syndrome.
- Mechanisms of gene action in disorders of the endocrine glands.
- A familial neurological disease with symptomatic response to levodopa.
- Report of five unrelated patients with a small, metacentric, extra chromosome or fragment.
- Genetics and malignancy. Genetics and malignant disease.
- Linear sebaceous nevus syndrome. A hamartoma variant.
- Subacute encephalitis and congenital hypogammaglobulinemia.
- Monozygotic twins with the Turner syndrome.
- A new mucopolysaccharidosis.
- Syndrome of bilateral pheochromocytoma, medullary Thyroid carcinoma and multiple neuromas. A possible regulatory defect in the differentiation of chromaffin tissue.
- The Noonan syndrome: a family study.
- A prospective study on Von Hippel-Lindau disease.
- Mesomelic dwarfism with hemivertebrae and small genitalia (the Robinow syndrome).
- Phenotype of malignancy: the mucosal neuroma syndrome.
- Endocrine genetics.
- Retinoblastoma and osteogenic sarcoma in siblings.
- Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency.
- Adult-onset hereditary cerebellar ataxia and neurosensory deafness.
- Beckwith-Wiedemann syndrome. Wilms'' tumor, cardiac hamartoma, persistent visceromegaly, and glomeruloneogenesis in a 2-year-old boy.
- Genetic aspects of the Z-E syndrome: prospective studies in two kindred; antral gastrin cell hyperplasia.
- Late onset ataxia, rigidity, and peripheral neuropathy. A familial syndrome with variable therapeutic response to levodopa.
- Chondroitin-6-sulfate mucopoly-saccharidosis in conjunction with lymphopenia, defective cellular immunity and the nephrotic syndrome.
- Benign, recessively inherited choreo-athetosis of early onset.
- The Roberts syndrome.
- ABO blood groups and Huntington''s choera.
- Immunologic deficiency in the congenital rubella syndrome.
- Immunoglobulins in congenital hypogammaglobulinemia.
- Paternal immunoglobulin Abnormalities in congenital hypogammaglobulinemia.
- Familial tumor endocrinopathies.
- X-linked congenital panHypopituitarism.
- Chondroitin-6-sulphaturia, defective cellular immunity, and nephrotic syndrome.
- Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females.
- Partial 15q trisomy: report of three siblings.
- Endocrine studies in a male patient with choriocarcinoma and gynecomastia.
- Proximal 3p deletion in renal cell carcinoma cells from a patient with von Hippel-Lindau disease.
- Dominantly inherited renal adysplasia.
- Nasopharyngeal carcinoma, aplastic anemia, and various malignancies in a family: possible role of Epstein-Barr virus.
- Androblastomas and Thyroid disease in postmenopausal sisters.
- Multiple endocrine neoplasia: search for the oncogenic trigger.
- Ehlers-Danlos syndrome: a new oculo-scoliotic type with associated polyneuropathy?
- Unknown syndrome in sibs: microcephaly, seizures, mental retardation, congenital heart disease, and skeletal Abnormalities.
- Persistent Mullerian duct syndrome: report of two boys with associated crossed testicular ectopia.
- Multiple endocrine neoplasia: how many syndromes?
- Hypomandibular faciocranial dysostosis: report of an affected sib and follow-up.
- HyperThyroidism. The clinical spectrum.
- Case report: breast Cancer in males--a genetic consideration.
- Genetics in cystic kidney disease.
- A crossover in the HL-A system traced through three generations.
- Familial acute myelogenous leukemia with associated C-monosomy in two affected members.
- Heterogeneity in the campomelic syndromes: long and short bone varieties.
Schools
Stanford University
University of Kansas School of Medicine
University Of Ks Med Center
Conditions Treated
- Abnormal Thyroid
- Hyperlipidemia
- HyperparaThyroidism
- Hypopituitarism
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Doctors Specialties
- Endocrinology
Accepted Insurances
Education
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University of Kansas School of Medicine
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