|1.||Jüppner, Harald: 4 articles (04/2015 - 01/2005)|
|2.||Kottler, Marie-Laure: 3 articles (05/2015 - 09/2013)|
|3.||Van Geet, Chris: 3 articles (04/2012 - 12/2008)|
|4.||Freson, Kathleen: 3 articles (04/2012 - 12/2008)|
|5.||Izzi, Benedetta: 3 articles (04/2012 - 12/2008)|
|6.||de Zegher, Francis: 3 articles (04/2012 - 12/2008)|
|7.||Thys, Chantal: 3 articles (04/2012 - 12/2008)|
|8.||Wittevrongel, Christine: 3 articles (04/2012 - 12/2008)|
|9.||Richard, Nicolas: 2 articles (04/2015 - 09/2013)|
|10.||de Nanclares, Guiomar Pérez: 2 articles (11/2014 - 12/2008)|
01/01/1997 - "In this study, we administered tests of odor detection, identification, and memory to (i) 13 patients with Type Ia PHP; (ii) 8 patients with Type Ib PHP; (iii) 7 patients with pseudopseudohypoparathyroidism (PPHP); and (iv) 3 sets of normal controls matched to these groups on the basis of age, gender, and smoking history. "
05/01/2015 - "If the alteration is on the paternal allele, there are few clinical signs with no hormonal resistance and the phenotype is known as pseudopseudo hypoparathyroidism (pseudo-PPHP). "
03/01/2015 - "Paternally inherited inactivating mutations lead to isolated AHO signs characterizing pseudo-pseudohypoparathyroidism (PPHP). "
09/01/2014 - "A 51-year-old Caucasian female had been diagnosed of pseudo-pseudohypoparathyroidism (PPHP) in 1989. "
01/01/2014 - "We reported a 12- year- old girl with unusual clinical manifestations of Pseudopseudohypoparathyroidism(PPHP). "
01/01/2015 - "AHO manifests in two different phenotypes, pseudohypoparathyroidism type Ia (PHP-Ia) and pseudopsedohypoparthyroidim (PPHP), which may happen in the same family members. "
06/01/2000 - "Although HAM rarely accompanies pseudohypoparathyroidism (PHP), there are few reported cases of HAM associated with PPHP. "
10/01/1993 - "Further observations are necessary to define the frequency and significance of GH deficiency and the role of GH replacement therapy in pseudohypoparathyroidism- and PPHP-associated short stature."
01/01/2014 - "An inactivating mutation in the GNAS gene causes either pseudohypoparathyroidism 1a (PHP1A) when it is maternally inherited or pseudopseudohypoparathyroidism (PPHP) when it is paternally inherited. "
09/01/2013 - "Heterozygous GNAS inactivating mutations cause pseudohypoparathyroidism type Ia (PHP-Ia) when maternally inherited and pseudopseudohypoparathyroidism (PPHP)/progressive osseous heteroplasia (POH) when paternally inherited. "
11/01/2014 - "TRPS was mistakenly identified as PHP/PPHP because of the coexistence of obesity and brachydactyly, with PTH resistance in one of the cases. "
12/01/2004 - "Our results provide evidence for the absence of Gsalpha imprinting in human bone and fat and suggest that the clinical finding of osteodystrophy and obesity in PHP Ia and PPHP patients despite the presence of a normal Gsalpha allele is likely due to Gsalpha haploinsufficiency in these tissues."
08/01/2007 - "Recently it was reported that obesity is a more prominent feature in pseudohypoparathyroidism type I a than in PPHP. "
10/01/2010 - "If the alteration is on the paternal allele, there are few clinical signs with no hormonal resistance and the phenotype is known as pseudo-pseudo-hypoparathyroidism (PPHP). "
12/01/1983 - "Calcitonin (CT) levels were determined in urine specimens from normal subjects and patients with pseudohypoparathyroidism type I (PHP), idiopathic hypoparathyroidism (IHP), pseudopseudohypoparathyroidism (PPHP), and surgical hypoparathyroidism (SHP). "
01/01/1993 - "AHO refers to the phenotype of the syndromes of pseudo-hypoparathyroidism (PHP) type Ia and pseudopseudohypoparathyroidism (PPHP), both considered genetically related variants with a defect of the alpha subunit of the stimulatory G protein of adenylate cyclase, necessary for the action of parathyroid and other hormones using cyclic AMP as an intracellular second messenger. "
|2.||Albright's hereditary osteodystrophy
|3.||Parathyroid Hormone (Parathormone)
|4.||GTP-Binding Proteins (G-Protein)
|6.||Adenylate Cyclase (Adenylyl Cyclase)