|1.||Hendy, Geoffrey N: 8 articles (01/2013 - 03/2002)|
|2.||Marx, Stephen J: 6 articles (02/2015 - 11/2002)|
|3.||Cole, David E C: 6 articles (01/2013 - 03/2002)|
|4.||Brown, Edward M: 5 articles (01/2015 - 03/2002)|
|5.||Canaff, Lucie: 5 articles (04/2010 - 03/2002)|
|6.||Breitwieser, Gerda E: 3 articles (01/2015 - 07/2009)|
|7.||Hannan, Fadil M: 3 articles (07/2014 - 06/2013)|
|8.||Thakker, Rajesh V: 3 articles (07/2014 - 06/2013)|
|9.||Brixen, Kim: 3 articles (06/2014 - 12/2008)|
|10.||Levine, Michael A: 3 articles (01/2014 - 11/2009)|
|1.||Hypercalcemia (Milk Alkali Syndrome)
01/01/2012 - "We report a 9-year-old female with persistent hypercalcemia in several routine blood analyses, who was diagnosed with familial hypocalciuric hypercalcemia after genetic studies were performed. "
03/01/2012 - "Familial hypocalciuric hypercalcemia is a rare cause of hypercalcemia that usually presents with asymptomatic hypercalcemia. "
03/01/2011 - "Benign familial hypocalciuric hypercalcemia is a small but important cause of hypercalcemia, especially in the younger population. "
01/01/2011 - "Familial hypocalciuric hypercalcemia (FHH) is a cause of hypercalcemia with autosomal dominant pattern of inheritance and high penetrance. "
08/01/2010 - "One rare cause of hypercalcemia in the child is familial hypocalciuric hypercalcemia (also termed familial benign hypercalcemia). "
07/01/2013 - "Because the clinical features of familial hypocalciuric hypercalcemia (FHH) overlap significantly with those of primary hyperparathyroidism (PHPT), various means of differentiating between the two diseases have been suggested. "
07/01/2013 - "Differentiating familial hypocalciuric hypercalcemia from primary hyperparathyroidism."
05/01/2012 - "To discuss the unusual occurrence of both familial hypocalciuric hypercalcemia (FHH) and primary hyperparathyroidism in the same patient and to explore potential mechanisms of association and issues related to clinical management. "
05/01/2012 - "Primary hyperparathyroidism and familial hypocalciuric hypercalcemia: relationships and clinical implications."
10/01/2011 - "Forearm bone mineral density in familial hypocalciuric hypercalcemia and primary hyperparathyroidism: a comparative study."
06/01/1984 - "The significantly reduced percent parenchyma in glands from patients with familial hypocalciuric hypercalcemia further suggests that the condition is not uniformly accompanied by typical parathyroid hyperplasia and should not be thought of as merely a variant of the latter."
08/12/1982 - "Familial hypocalciuric hypercalcemia: the relation to primary parathyroid hyperplasia."
03/01/1981 - "Simple quantitative analyses were useful in identifying parathyroid hyperplasia in the group with familial hypocalciuric hypercalcemia."
03/01/1981 - "Mild parathyroid hyperplasia was a feature in most patients with familial hypocalciuric hypercalcemia who had undergone neck surgery. "
06/01/1984 - "The histologic characteristics of the parathyroid glands in familial benign hypercalcemia (familial hypocalciuric hypercalcemia) are disputed, some finding parathyroid hyperplasia and others finding no abnormalities. "
10/01/2013 - "DNA sequence analysis of the CASR gene was undertaken in autosomal dominant hypoparathyroidism and familial hypocalciuric hypercalcemia Japanese patients, and the functional consequences for the Gi-MAPK pathway and cell surface expression of CASR were determined. "
02/01/2001 - "Mutations of the CASR gene cause familial hypocalciuric hypercalcemia or autosomal dominant hypoparathyroidism, depending on whether they decrease or increase, respectively, ligand binding to the receptor protein. "
05/01/2001 - "CaR cloning was immediately followed by the association of genetic human diseases with inactivating and activating CaR mutations: familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism are caused by CaR-inactivating mutations, whereas autosomal dominant hypoparathyroidism is secondary to CaR-activating mutations. "
10/01/2013 - "Activating mutations in the calcium-sensing receptor (CASR) gene cause autosomal dominant hypoparathyroidism, and heterozygous inactivating CASR mutations cause familial hypocalciuric hypercalcemia. "
03/22/2012 - "Calcium metabolic disorders like familial hypocalciuric hypercalcemia (FHH) and autosomal dominant familial isolated hypoparathyroidism (FIH) can be caused by rare variants of the calcium sensing receptor gene (CASR). "
|4.||Parathyroid Hormone (Parathormone)
|5.||GTP-Binding Proteins (G-Protein)
|3.||Total Parenteral Nutrition