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FRONTIERS IN ENDOCRINOLOGY, ISSN 1664-2392, 08/2019, Volume 10
Pseudohypoparathyroidism (PHP) is a rare endocrine disorder derived from the defective activation of the cAMP pathway by the parathyroid hormone secondary to... 
brachydactyly-mental retardation syndrome | pseudohypoparathyroidism | DIAGNOSIS | GENE | MENTAL-RETARDATION SYNDROME | ENDOCRINOLOGY & METABOLISM | GNAS | 2q37 deletion | Albright hereditary osteodystrophy | Parathyroid hormone | Genetic aspects
Journal Article
Journal of clinical and diagnostic research : JCDR, ISSN 2249-782X, 10/2014, Volume 8, Issue 10, pp. ZD28 - ZD30
A dental practitioner with an eagle's eye can diagnose many hidden disease through careful examination of the oral cavity. One such hereditary metabolic... 
Albright hereditary osteodystrophy (AHO) | Dentistry Section | Brachydactyly | Pseudohypoparathyroidism
Journal Article
Journal Article
Clinical Case Reports, ISSN 2050-0904, 10/2018, Volume 6, Issue 10, pp. 1933 - 1940
Key Clinical Message Germline loss‐of‐function GNAS mutations are associated with multiple phenotypes, depending on the parental origin of the mutant allele.... 
pseudohypoparathyroidism | inactivating PTH/PTHrP signaling disorders | severe phenotype | Albright's hereditary osteodystrophy | GNAS mutation
Journal Article
Indian Journal of Pediatrics, ISSN 0019-5456, 02/2006, Volume 73, Issue 2, pp. 153 - 156
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 2013, Volume 7, Issue 1, pp. 111 - 111
We report for the first time the case of a patient with Albright hereditary osteodystrophy and pseudopseudohypoparathyroidism who underwent a Roux-en-Y gastric... 
Roux-en-Y gastric bypass | Bone | Calcium | Pseusopseudohypoparathyroidism | Albright hereditary osteodystrophy | Type 2 diabetes | Obesity | Overweight persons | Vitamin D | Surgery | Calcifediol | Alfacalcidol | Bone diseases
Journal Article
Experimental and Clinical Endocrinology & Diabetes, ISSN 0947-7349, 02/2010, Volume 118, Issue 2, pp. 127 - 132
Abstract OBJECTIVE: Albright hereditary osteodystrophy (AHO) and Pseudohypoparathyroidism type Ia (PHPIa) are caused by an inherited deficiency of Gsα, encoded... 
Article | STIMULATORY G-PROTEIN | IDENTIFICATION | CONTROL REGION | GNAS mutations | HORMONE RESISTANCE | MESSENGER-RNA | METABOLISM | Pseudohypoparathyroidism type Ia | ENDOCRINOLOGY & METABOLISM | PROGRESSIVE OSSEOUS HETEROPLASIA | Albright hereditary osteodystrophy | INACTIVATING MUTATIONS | SUBUNIT
Journal Article
The Indian Journal of Pediatrics, ISSN 0019-5456, 2/2006, Volume 73, Issue 2, pp. 153 - 156
Albright’s hereditary osteodystrophy is a rare inherited metabolic disorder characterized by a typical phenotype. It may be associated with or without... 
Pediatrics | Medicine & Public Health | Albright’s hereditary osteodystrophy | Pseudo-pseudohypoparathyroidism | Gynecology | Pseudohypoparathyroidism | Gs alpha activity
Journal Article
ARCHIVOS ARGENTINOS DE PEDIATRIA, ISSN 0325-0075, 04/2010, Volume 108, Issue 2, pp. E24 - E27
Albright's hereditary osteodystrophy includes an heterogeneous group of genetic diseases, including the pseudohypoparathyroidism type Ia and... 
PEDIATRICS | hereditary osteodystrophy | children | Albright's syndrome | MUTATION | Fibrous Dysplasia, Polyostotic - diagnosis | Humans | Adolescent | Female | Infant | Male | Child
Journal Article
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