مرض ماهفاش (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "مرض ماهفاش" in Arabic language version.

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10nih.gov

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9doi.org

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1web.archive.org

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doi.org

"Mahvash Disease: 10 Years After Discovery". Pancreas. ج. 47 ع. 5: 511–515. 2018. DOI:10.1097/MPA.0000000000001044. PMID:29702528.
"Homozygous P86S mutation of the human glucagon receptor is associated with hyperglucagonemia, alpha cell hyperplasia, and islet cell tumor". Pancreas. ج. 38 ع. 8: 941–6. نوفمبر 2009. DOI:10.1097/MPA.0b013e3181b2bb03. PMID:19657311.
"Glucagon cell hyperplasia and neoplasia with and without glucagon receptor mutations". The Journal of Clinical Endocrinology and Metabolism. ج. 100 ع. 5: E783-8. مايو 2015. DOI:10.1210/jc.2014-4405. PMID:25695890.
"Pancreatic α-cell hyperplasia and hyperglucagonemia due to a glucagon receptor splice mutation". Endocrinology, Diabetes & Metabolism Case Reports. ج. 2016: 0081. 2016. DOI:10.1530/EDM-16-0081. PMID:27933176.
"Hypercalcemia in Glucagon Cell Hyperplasia and Neoplasia (Mahvash Syndrome): A New Association". The Journal of Clinical Endocrinology and Metabolism. ج. 103 ع. 9: 3119–3123. سبتمبر 2018. DOI:10.1210/jc.2018-01074. PMID:30032256.
"GCGR is identified by newborn screening of elevated arginine". Molecular Genetics and Metabolism Reports. ج. 17: 46–52. ديسمبر 2018. DOI:10.1016/j.ymgmr.2018.09.006. PMID:30294546.
"Pancreatic α-cell hyperplasia: facts and myths". The Journal of Clinical Endocrinology and Metabolism. ج. 99 ع. 3: 748–56. مارس 2014. DOI:10.1210/jc.2013-2952. PMID:24285676.
"Glucagon Couples Hepatic Amino Acid Catabolism to mTOR-Dependent Regulation of α-Cell Mass". Cell Reports. ج. 12 ع. 3: 495–510. يوليو 2015. DOI:10.1016/j.celrep.2015.06.034. PMID:26166562. {{استشهاد بدورية محكمة}}: الوسيط |إظهار المؤلفين=6 غير صالح (مساعدة)
"Pancreatic neuroendocrine tumors in glucagon receptor-deficient mice". PLOS One. ج. 6 ع. 8: e23397. 2011. DOI:10.1371/journal.pone.0023397. PMID:21853126.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)

nih.gov

pubmed.ncbi.nlm.nih.gov

"Mahvash Disease: 10 Years After Discovery". Pancreas. ج. 47 ع. 5: 511–515. 2018. DOI:10.1097/MPA.0000000000001044. PMID:29702528.
"Homozygous P86S mutation of the human glucagon receptor is associated with hyperglucagonemia, alpha cell hyperplasia, and islet cell tumor". Pancreas. ج. 38 ع. 8: 941–6. نوفمبر 2009. DOI:10.1097/MPA.0b013e3181b2bb03. PMID:19657311.
"Glucagon cell hyperplasia and neoplasia with and without glucagon receptor mutations". The Journal of Clinical Endocrinology and Metabolism. ج. 100 ع. 5: E783-8. مايو 2015. DOI:10.1210/jc.2014-4405. PMID:25695890.
"Pancreatic α-cell hyperplasia and hyperglucagonemia due to a glucagon receptor splice mutation". Endocrinology, Diabetes & Metabolism Case Reports. ج. 2016: 0081. 2016. DOI:10.1530/EDM-16-0081. PMID:27933176.
"Hypercalcemia in Glucagon Cell Hyperplasia and Neoplasia (Mahvash Syndrome): A New Association". The Journal of Clinical Endocrinology and Metabolism. ج. 103 ع. 9: 3119–3123. سبتمبر 2018. DOI:10.1210/jc.2018-01074. PMID:30032256.
"GCGR is identified by newborn screening of elevated arginine". Molecular Genetics and Metabolism Reports. ج. 17: 46–52. ديسمبر 2018. DOI:10.1016/j.ymgmr.2018.09.006. PMID:30294546.
"Pancreatic α-cell hyperplasia: facts and myths". The Journal of Clinical Endocrinology and Metabolism. ج. 99 ع. 3: 748–56. مارس 2014. DOI:10.1210/jc.2013-2952. PMID:24285676.
"Glucagon Couples Hepatic Amino Acid Catabolism to mTOR-Dependent Regulation of α-Cell Mass". Cell Reports. ج. 12 ع. 3: 495–510. يوليو 2015. DOI:10.1016/j.celrep.2015.06.034. PMID:26166562. {{استشهاد بدورية محكمة}}: الوسيط |إظهار المؤلفين=6 غير صالح (مساعدة)
"Pancreatic neuroendocrine tumors in glucagon receptor-deficient mice". PLOS One. ج. 6 ع. 8: e23397. 2011. DOI:10.1371/journal.pone.0023397. PMID:21853126.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)

rarediseases.info.nih.gov

"Mahvash disease, Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. معاهد الصحة الوطنية الأمريكية. مؤرشف من الأصل في 2018-12-09. اطلع عليه بتاريخ 2018-12-08.

web.archive.org

"Mahvash disease, Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. معاهد الصحة الوطنية الأمريكية. مؤرشف من الأصل في 2018-12-09. اطلع عليه بتاريخ 2018-12-08.