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المساهمون: Faggiano, Antongiulio, L. B., Tavare, L., Tauchmanovà, Milone, Francesco, G., Mansueto, V., Ramundo, DEL BASSO DE CARO, Marialaura, G., Lombardi, DE ROSA, Gaetano, Colao, Annamaria

المصدر: Clinical Endocrinology. 69:756-762

مصطلحات موضوعية: Adult, Male, Parathyroidectomy, endocrine system, medicine.medical_specialty, Hypercalcaemia, Antineoplastic Agents, Hormonal, endocrine system diseases, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, Octreotide, Antineoplastic Agents, Drug Administration Schedule, Young Adult, Endocrinology, Duodenal Neoplasms, Internal medicine, Multiple Endocrine Neoplasia Type 1, medicine, Humans, multiple endocrine neoplasia, Hypercalciuria, Aged, Hyperparathyroidism, Hormonal, business.industry, Somatostatin receptor, Delayed-Action Preparations, Female, Hyperparathyroidism, Primary, Middle Aged, Neuroendocrine Tumors, Pancreatic Neoplasms, Somatostatin, medicine.disease, MEN1, business, Primary, hormones, hormone substitutes, and hormone antagonists, Primary hyperparathyroidism, medicine.drug

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54b7529ccb7ca2024e813b4a9c5e899eTest
https://doi.org/10.1111/j.1365-2265.2008.03301.xTest

7

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1

المؤلفون: Zsuzsa Valkusz, Attila Patócs, Miklós Tóth, Katalin Balogh, László Hunyady, Károly Rácz, Peter Gergics

المصدر: Clinical Endocrinology. 67:727-734

مصطلحات موضوعية: Adult, Male, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, medicine.medical_specialty, Adolescent, endocrine system diseases, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Molecular Sequence Data, Mutation, Missense, Biology, Gene mutation, medicine.disease_cause, Polymerase Chain Reaction, Evolution, Molecular, Endocrinology, Germline mutation, Internal medicine, Multiple Endocrine Neoplasia Type 1, medicine, Humans, Missense mutation, MEN1, Genetic Testing, Multiple endocrine neoplasia, Germ-Line Mutation, Aged, Aged, 80 and over, Hungary, Mutation, Polymorphism, Genetic, Base Sequence, Middle Aged, medicine.disease, Phenotype, Case-Control Studies, MEN1 Gene Mutation, Female, Sequence Alignment, Primary hyperparathyroidism

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c517f06a9514ce3b9cdb657386c84e8cTest
https://doi.org/10.1111/j.1365-2265.2007.02953.xTest

8

Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas

المؤلفون: Gert Jan Fleuren, T. van Wezel, Bin Tean Teh, Carola J. Haven, Hans Morreau, Min-Han Tan, M. van Puijenbroek

المصدر: Clinical Endocrinology. 67:370-376

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pathology, endocrine system diseases, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Mutation, Missense, Loss of Heterozygosity, Biology, Frameshift mutation, Cohort Studies, Loss of heterozygosity, Endocrinology, Germline mutation, Proto-Oncogene Proteins, Internal medicine, Multiple Endocrine Neoplasia Type 1, Carcinoma, medicine, Humans, Missense mutation, MEN1, Frameshift Mutation, Multiple endocrine neoplasia, Aged, Biological Specimen Banks, Netherlands, Aged, 80 and over, Paraffin Embedding, Tumor Suppressor Proteins, Middle Aged, medicine.disease, Parathyroid Neoplasms, Parathyroid carcinoma, Cancer research, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1992c70b4bf003b81d8e251103e23f12Test
https://doi.org/10.1111/j.1365-2265.2007.02894.xTest

9

Growth hormone-binding protein related immunoreactivity is regulated by the degree of insulinopenia in diabetes mellitus

المؤلفون: K. Kellner, T. Zilkens, G. H. Scholz, H. Schmidt-Gayk, J. Kratzsch, T. Selisko

المصدر: Clinical Endocrinology. 44:673-678

مصطلحات موضوعية: Adult, Male, endocrine system, medicine.medical_specialty, endocrine system diseases, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, Growth hormone receptor, Biology, Insulin-like growth factor, Endocrinology, Growth hormone-binding protein, Internal medicine, Diabetes mellitus, Diabetes Mellitus, medicine, Humans, Insulin, Insulin-Like Growth Factor I, Aged, Proinsulin, C-Peptide, nutritional and metabolic diseases, Receptors, Somatotropin, Middle Aged, medicine.disease, Insulin-Like Growth Factor Binding Protein 1, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Growth Hormone, Female, Animal studies, Carrier Proteins, hormones, hormone substitutes, and hormone antagonists, Hormone

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c804201213d52f02aed43a241081f6feTest
https://doi.org/10.1046/j.1365-2265.1996.672494.xTest

10

Germline mutation of HRPT2 in patients with HPT

المصدر: Clinical Endocrinology. 65:9-16

مصطلحات موضوعية: Adenoma, Adult, Male, Pathology, medicine.medical_specialty, Genotype, endocrine system diseases, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Loss of Heterozygosity, Biology, Methylation, Endocrinology, Germline mutation, jaw tumor, Internal medicine, Multiple Endocrine Neoplasia Type 1, medicine, Humans, Missense mutation, Genes, Tumor Suppressor, MEN1, Frameshift Mutation, Promoter Regions, Genetic, Germ-Line Mutation, Aged, Parathyroid adenoma, Hyperparathyroidism, parathyroid tumor, Tumor Suppressor Proteins, FIHP, Sequence Analysis, DNA, Middle Aged, Hyperparathyroidism, Primary, medicine.disease, Jaw Neoplasms, Hyperparathyroidism-Jaw Tumor Syndrome, Pedigree, HRPT2, Parathyroid Neoplasms, Parathyroid carcinoma, HPT-JT, Mutation, Female, Receptors, Calcium-Sensing, Gene Deletion, Primary hyperparathyroidism, Microsatellite Repeats

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c5d30a0279cffa260dbd8757074096Test
https://doi.org/10.1111/j.1365-2265.2006.02534.xTest

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