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 *

131 related articles for article (PubMed ID: 27703483)

  • 1. The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?
    Kashani P; Roy M; Gillis L; Ajani O; Samaan MC
    Case Rep Med; 2016; 2016():7645938. PubMed ID: 27703483
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cutaneous nodules and a novel
    Li YL; Han T; Hong F
    World J Clin Cases; 2020 Feb; 8(3):587-593. PubMed ID: 32110670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early Diagnosis of Pseudohypoparathyroidism before the Development of Hypocalcemia in a Young Infant.
    Hwang SK; Shim YJ; Oh SH; Jang KM
    Children (Basel); 2022 May; 9(5):. PubMed ID: 35626900
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pseudohypoparathyroidism type Ia: a novel GNAS mutation in a Brazilian boy presenting with an early primary hypothyroidism.
    Alves C; Sampaio S; Barbieri AM; Mantovani G
    J Pediatr Endocrinol Metab; 2013; 26(5-6):557-60. PubMed ID: 23412865
    [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. Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy.
    Lin MH; Numbenjapon N; Germain-Lee EL; Pitukcheewanont P
    J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):911-8. PubMed ID: 25894639
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones.
    Winter J; Hiort O; Hermanns P; Thiele S; Pohlenz J
    J Pediatr Endocrinol Metab; 2011; 24(5-6):297-301. PubMed ID: 21823526
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene.
    Şahin S; Hiort O; Thiele S; Evliyaoğlu O; Tüysüz B
    J Clin Res Pediatr Endocrinol; 2017 Mar; 9(1):74-79. PubMed ID: 27425121
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levels.
    Reis MT; Cattani A; Mendonca BB; Corrêa PH; Martin RM
    Arq Bras Endocrinol Metabol; 2010 Nov; 54(8):728-31. PubMed ID: 21340160
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 22-year-old woman with hypocalcemia and clinical features of albright hereditary osteodystrophy diagnosed with sporadic pseudohypoparathyroidism type Ib using a methylation-specific multiplex ligation-dependent probe amplification assay.
    Zeniya S; Yuno A; Watanabe T; Usui T; Moriki Y; Uno Y; Miake H
    Intern Med; 2014; 53(9):979-86. PubMed ID: 24785890
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A pseudohypoparathyroidism type Ia patient with normocalcemia.
    Tamada Y; Kanda S; Suzuki H; Tajima T; Nishiyama T
    Endocr J; 2008 Mar; 55(1):169-73. PubMed ID: 18250541
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Genetic analysis and evaluation of resistance to thyrotropin and growth hormone-releasing hormone in pseudohypoparathyroidism type Ib.
    Mantovani G; Bondioni S; Linglart A; Maghnie M; Cisternino M; Corbetta S; Lania AG; Beck-Peccoz P; Spada A
    J Clin Endocrinol Metab; 2007 Sep; 92(9):3738-42. PubMed ID: 17595244
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Clinical features of two cases of pseudohypoparathyroidism (ia and ib) and molecular analysis of GNAS].
    Domínguez García A; Castaño González LA; Pérez-Nanclares G; Quinteiro González S; Caballero Fernández E
    An Pediatr (Barc); 2013 Nov; 79(5):319-24. PubMed ID: 23623851
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recent advances in GNAS epigenetic research of pseudohypoparathyroidism.
    Izzi B; Van Geet C; Freson K
    Curr Mol Med; 2012 Jun; 12(5):566-73. PubMed ID: 22300135
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical characterization and identification of two novel mutations of the GNAS gene in patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism.
    Jin HY; Lee BH; Choi JH; Kim GH; Kim JK; Lee JH; Yu J; Yoo JH; Ko CW; Lim HH; Chung HR; Yoo HW
    Clin Endocrinol (Oxf); 2011 Aug; 75(2):207-13. PubMed ID: 21521295
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chiari type 1 anomaly in pseudohypoparathyroidism type Ia: pathogenetic hypothesis.
    Martínez-Lage JF; Guillén-Navarro E; López-Guerrero AL; Almagro MJ; Cuartero-Pérez B; de la Rosa P
    Childs Nerv Syst; 2011 Dec; 27(12):2035-9. PubMed ID: 21994050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GNAS locus and pseudohypoparathyroidism.
    Bastepe M; Jüppner H
    Horm Res; 2005; 63(2):65-74. PubMed ID: 15711092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.