|1.||Weinstein, Lee S: 9 articles (09/2012 - 06/2002)|
|2.||Hiort, Olaf: 8 articles (03/2015 - 04/2003)|
|3.||Levine, Michael A: 8 articles (10/2009 - 01/2002)|
|4.||Germain-Lee, Emily L: 7 articles (07/2015 - 09/2003)|
|5.||Chen, Min: 7 articles (09/2012 - 06/2002)|
|6.||Bastepe, Murat: 6 articles (06/2015 - 10/2003)|
|7.||Ahrens, Wiebke: 5 articles (06/2007 - 04/2003)|
|8.||Jüppner, Harald: 4 articles (10/2015 - 10/2003)|
|9.||Mantovani, Giovanna: 4 articles (05/2015 - 02/2010)|
|10.||Garin, Intza: 4 articles (04/2015 - 11/2008)|
10/01/2011 - "A PubMed search was used to identify the available studies (main query terms: pseudohypoparathyroidism; Albright hereditary osteodystrophy; GNAS; GNAS1; progressive osseous heteroplasia). "
02/01/2005 - "Pseudohypoparathyroidism associated with Albright's hereditary osteodystrophy was diagnosed by biochemical, hormonal and radiographic studies. "
01/01/2002 - "We conducted clinical and biological studies including screening for mutations in the gene encoding the alpha subunit of G(s) (GNAS1) in 30 subjects (21 unrelated families) with Albright's hereditary osteodystrophy (AHO), pseudohypoparathyroidism (PHP); and decreased erythrocyte G(s) activity (PHP-Ia; n = 19); AHO and decreased erythrocyte G(s) activity (isolated AHO; n = 10); or AHO, hormonal resistance, and normal erythrocyte G(s) activity (PHP-Ic; n = 1). "
07/01/2015 - "Reports of patients with mild POH with Albright hereditary osteodystrophy (AHO), specifically pseudohypoparathyroidism type Ia (PHP Ia) with hormonal resistance, suggest the possibility of a common molecular basis. "
06/01/2014 - "We describe a Chinese woman and her son, who presented with different symptoms of pseudohypoparathyroidism and clinically manifested different degree of Albright's hereditary osteodystrophy. "
02/01/1964 - "PSEUDO-PSEUDOHYPOPARATHYROIDISM (ALBRIGHT'S HEREDITARY OSTEODYSTROPHY): A FAMILY STUDY."
01/01/2013 - "After a Roux-en-Y gastric bypass, patients with Albright hereditary osteodystrophy associated with pseudopseudohypoparathyroidism need long-term follow-up on nutritional and metabolic issues."
01/01/2013 - "This is the first case of Roux-en-Y gastric bypass described in a patient with pseudopseudohypoparathyroidism showing that such a procedure seems to be safe in obese patients with Albright hereditary osteodystrophy and pseudopseudohypoparathyroidism if appropriately followed up. "
01/01/2013 - "A 26-year-old obese Caucasian woman with Albright hereditary osteodystrophy with pseudopseudohypoparathyroidism (heterozygous mutation (L272F) in GNAS1 exon 10 on molecular analysis) was treated with gastric bypass. "
01/01/2013 - "We report for the first time the case of a patient with Albright hereditary osteodystrophy and pseudopseudohypoparathyroidism who underwent a Roux-en-Y gastric bypass. "
08/08/2014 - "Albright's Hereditary Osteodystrophy (AHO) was the first inherited disease associated with loss-of-function mutations in a G protein (Gαs) and other studies revealed gain-of-function Gα mutations in cancer. "
09/01/2007 - "Loss-of-function and gain-of-function mutations within Gsalpha-coding GNAS exons are found in various human disorders, including Albright's hereditary osteodystrophy, pseudohypoparathyroidism, fibrous dysplasia of bone, and some tumors of different origin. "
10/01/1993 - "Such G protein mutations play a role in the pathogenesis of several human diseases, including sporadic endocrine tumors, McCune-Albright syndrome, and Albright hereditary osteodystrophy."
05/01/1995 - "Mutations of heterotrimeric G proteins have been found in a number of endocrine tumors, the McCune-Albright syndrome, Albright's hereditary osteodystrophy, and a combination of precocious puberty and pseudohypoparathyroidism Ia. "
07/01/2002 - "In this study, we report a clinical case of a 17-year-old woman with Albright hereditary osteodystrophy, and we discuss her clinical, radiographic, and laboratory test characteristics together with the oral manifestations, and we correlate them with the characteristics found in the literature. "
07/01/2002 - "Oral manifestations of Albright hereditary osteodystrophy: a case report."
09/01/2013 - "In addition, she had several features similar to Albright's hereditary osteodystrophy including short stature, truncal obesity, round face, short neck, low intelligence (full IQ 84), and decreased memory. "
01/01/2013 - "Patients with Albright hereditary osteodystrophy (AHO) phenotype are usually seen in pediatric endocrinology policlinics when they are evaluated for short stature and/or obesity. "
01/01/2013 - "She had the classical features of Albright hereditary osteodystrophy: short stature (138cm), obesity (body mass index 49.5kg/m2), bilateral shortening of the fourth and fifth metacarpals, short neck, round and wide face with bombed front and small eyes. "
01/01/2013 - "We report a case of Albright hereditary osteodystrophy (AHO) in a three-year-old girl with a microduplication at 17q11.2. The child developed obesity within the first 6 months of life. "
09/01/2012 - "Heterozygous inactivating G(s)α mutations on the maternal allele result in obesity primarily due to reduced energy expenditure in Albright hereditary osteodystrophy patients and in mice. "
|1.||Parathyroid Hormone (Parathormone)
|2.||GTP-Binding Proteins (G-Protein)
|5.||Gs GTP-Binding Protein alpha Subunits (G(s)alpha)
|6.||Adenylate Cyclase (Adenylyl Cyclase)
|10.||GTP-Binding Protein alpha Subunits
|2.||Gastric Bypass (Roux-en-Y Gastric Bypass)