257 related articles for article (PubMed ID: 27467896)
1. Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases.
Kayemba-Kay's S; Tripon C; Heron A; Hindmarsh P
J Clin Res Pediatr Endocrinol; 2016 Dec; 8(4):432-438. PubMed ID: 27467896
[TBL] [Abstract][Full Text] [Related]
2. Establishment of diagnosis by bisulfite-treated methylation-specific PCR method and analysis of clinical characteristics of pseudohypoparathyroidism type 1b.
Kinoshita K; Minagawa M; Takatani T; Takatani R; Ohashi M; Kohno Y
Endocr J; 2011; 58(10):879-87. PubMed ID: 21836370
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis.
Pereda A; Garin I; ; Perez de Nanclares G
BMC Med Genet; 2018 Mar; 19(1):32. PubMed ID: 29499646
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Case report of GNAS epigenetic defect revealed by a congenital hypothyroidism.
Romanet P; Osei L; Netchine I; Pertuit M; Enjalbert A; Reynaud R; Barlier A
Pediatrics; 2015 Apr; 135(4):e1079-83. PubMed ID: 25802348
[TBL] [Abstract][Full Text] [Related]
8. Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder.
Turan S
J Clin Res Pediatr Endocrinol; 2017 Dec; 9(Suppl 2):58-68. PubMed ID: 29280743
[TBL] [Abstract][Full Text] [Related]
9. Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance.
Germain-Lee EL; Groman J; Crane JL; Jan de Beur SM; Levine MA
J Clin Endocrinol Metab; 2003 Sep; 88(9):4059-69. PubMed ID: 12970262
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Pseudohypoparathyroidism type 1a with congenital hypothyroidism.
Pinsker JE; Rogers W; McLean S; Schaefer FV; Fenton C
J Pediatr Endocrinol Metab; 2006 Aug; 19(8):1049-52. PubMed ID: 16995592
[TBL] [Abstract][Full Text] [Related]
12. Pseudohypoparathyroidism type 1A and morbid obesity in infancy.
Dekelbab BH; Aughton DJ; Levine MA
Endocr Pract; 2009 Apr; 15(3):249-53. PubMed ID: 19364695
[TBL] [Abstract][Full Text] [Related]
13. Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoption.
de Sanctis L; Giachero F; Mantovani G; Weber G; Salerno M; Baroncelli GI; Elli MF; Matarazzo P; Wasniewska M; Mazzanti L; Scirè G; Tessaris D;
Ital J Pediatr; 2016 Nov; 42(1):101. PubMed ID: 27871293
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Diagnosis and management of congenital hypothyroidism associated with pseudohypoparathyroidism.
Picard C; Decrequy A; Guenet D; Bursztejn AC; Toledano D; Richard N; Kottler ML
Horm Res Paediatr; 2015; 83(2):111-7. PubMed ID: 25591844
[TBL] [Abstract][Full Text] [Related]
16. GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance.
Linglart A; Carel JC; Garabédian M; Lé T; Mallet E; Kottler ML
J Clin Endocrinol Metab; 2002 Jan; 87(1):189-97. PubMed ID: 11788646
[TBL] [Abstract][Full Text] [Related]
17. [GNAS1 gene abnormality in pseudohypoparathyroidism I a].
Ozono K
Clin Calcium; 2007 Aug; 17(8):1214-9. PubMed ID: 17660618
[TBL] [Abstract][Full Text] [Related]
18. Progressive Development of PTH Resistance in Patients With Inactivating Mutations on the Maternal Allele of GNAS.
Usardi A; Mamoune A; Nattes E; Carel JC; Rothenbuhler A; Linglart A
J Clin Endocrinol Metab; 2017 Jun; 102(6):1844-1850. PubMed ID: 28323910
[TBL] [Abstract][Full Text] [Related]
19. Short stature, obesity, and growth hormone deficiency in pseudohypoparathyroidism type 1a.
Germain-Lee EL
Pediatr Endocrinol Rev; 2006 Apr; 3 Suppl 2():318-27. PubMed ID: 16675931
[TBL] [Abstract][Full Text] [Related]
20. Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5.
Savaş Erdeve Ş; Berberoğlu M; Şıklar Z; Evliyaoğlu O; Hiort O; Öcal G
J Clin Res Pediatr Endocrinol; 2010; 2(2):85-8. PubMed ID: 21274345
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
