These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 22299648)

  • 1. Linear skin atrophy preceding calcinosis cutis in pseudo-pseudohypoparathyroidism.
    Lau K; Willig RP; Hiort O; Hoeger PH
    Clin Exp Dermatol; 2012 Aug; 37(6):646-8. PubMed ID: 22299648
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Early manifestation of obesity and calcinosis cutis in infantile pseudohypoparathyroidism.
    Poomthavorn P; Zacharin M
    J Paediatr Child Health; 2006 Dec; 42(12):821-3. PubMed ID: 17096721
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation.
    Klaassens M; Blom EW; Schrander JJ; Ris-Stalpers C; Nieuwenhuijzen Kruseman AC; van Steensel MA; Schrander-Stumpel CT
    Br J Dermatol; 2010 Mar; 162(3):690-4. PubMed ID: 19863504
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.
    Riepe FG; Ahrens W; Krone N; Fölster-Holst R; Brasch J; Sippell WG; Hiort O; Partsch CJ
    Eur J Endocrinol; 2005 Apr; 152(4):515-9. PubMed ID: 15817905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progressive osseous heteroplasia-like heterotopic ossification in a male infant with pseudohypoparathyroidism type Ia: a case report.
    Gelfand IM; Hub RS; Shore EM; Kaplan FS; Dimeglio LA
    Bone; 2007 May; 40(5):1425-8. PubMed ID: 17321228
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
    Nakamoto JM; Sandstrom AT; Brickman AS; Christenson RA; Van Dop C
    Am J Med Genet; 1998 May; 77(4):261-7. PubMed ID: 9600732
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Albright hereditary osteodystrophy with hypothyroidism, normocalcemia, and normal Gs protein activity: a family presenting with congenital osteoma cutis.
    Izraeli S; Metzker A; Horev G; Karmi D; Merlob P; Farfel Z
    Am J Med Genet; 1992 Jul; 43(4):764-7. PubMed ID: 1621772
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Calcinosis cutis in Albright hereditary osteodystrophy: pseudohypoparathyroidism type Ia].
    Fölster-Holst R; Riepe FG; Ahrens W; Möller M; Brasch J; Partsch CJ; Hiort O; Sippell WG
    Hautarzt; 2006 Oct; 57(10):893-7. PubMed ID: 16270203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cutaneous ossification in Albright's hereditary osteodystrophy.
    Trüeb RM; Panizzon RG; Burg G
    Dermatology; 1993; 186(3):205-9. PubMed ID: 8453149
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Pseudohypoparathyroidism type Ia - a novel mutation].
    Reis Oliveira M; Oliveira Bandeira A; Rendeiro P; Silva Borges T; Cardoso H
    An Pediatr (Barc); 2010 Jun; 72(6):424-7. PubMed ID: 20409765
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of novel pathogenic variants and features in patients with pseudohypoparathyroidism and acrodysostosis, subtypes of the newly classified inactivating PTH/PTHrP signaling disorders.
    Truelove A; Mulay A; Prapa M; Casey RT; Adler AI; Offiah AC; Poole KES; Trotman J; Al Hasso N; Park SM
    Am J Med Genet A; 2019 Jul; 179(7):1330-1337. PubMed ID: 31041856
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two mutations of the Gsalpha gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia.
    Ishikawa Y; Tajima T; Nakae J; Nagashima T; Satoh K; Okuhara K; Fujieda K
    J Hum Genet; 2001; 46(7):426-30. PubMed ID: 11450852
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A positive genotype-phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo-pseudohypoparathyroidism and 33 newly identified mutations in the GNAS gene.
    Thiele S; Werner R; Grötzinger J; Brix B; Staedt P; Struve D; Reiz B; Farida J; Hiort O
    Mol Genet Genomic Med; 2015 Mar; 3(2):111-20. PubMed ID: 25802881
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel mutation in a patient with pseudohypoparathyroidism type Ia.
    Lee YS; Kim HK; Kim HR; Lee JY; Choi JW; Bae EJ; Oh PS; Park WI; Ki CS; Lee HJ
    Korean J Pediatr; 2014 May; 57(5):240-4. PubMed ID: 25045367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetics of pseudohypoparathyroidism: bases for proper genetic counselling.
    de Nanclares GP; Fernández-Rebollo E; Gaztambide S; Castaño L
    Endocrinol Nutr; 2008 Dec; 55(10):476-83. PubMed ID: 22980463
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis.
    Lubell T; Garzon M; Anyane Yeboa K; Shah B
    J Clin Res Pediatr Endocrinol; 2009; 1(5):244-7. PubMed ID: 21274302
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Osteoma cutis as the presenting feature of albright hereditary osteodystrophy associated with pseudopseudohypoparathyroidism.
    Jeong KH; Lew BL; Sim WY
    Ann Dermatol; 2009 May; 21(2):154-8. PubMed ID: 20523775
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple miliary osteoma cutis of the face associated with Albright hereditary osteodystrophy in the setting of acne vulgaris: a case report.
    Caravaglio JV; Gupta R; Weinstein D
    Dermatol Online J; 2017 Mar; 23(3):. PubMed ID: 28329522
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Osteoma cutis in pseudohypoparathyroidism.
    Sethuraman G; Malhotra AK; Khaitan BK; Kumar R; Sharma VK; Kabra M; Singh MK
    Clin Exp Dermatol; 2006 Mar; 31(2):225-7. PubMed ID: 16487097
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.