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Journal Abstract Search

159 related items for PubMed ID: 21229336

  • 1. Intraarticular heterotopic ossification as the initial manifestation in a child with pseudohypoparathyroidism 1a.
    Sarathi V, Patil A, Wade R, Bandgar TR, Shah NS.
    Indian J Pediatr; 2011 Jun; 78(6):745-8. PubMed ID: 21229336
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  • 2. Cutaneous ossification in Albright's hereditary osteodystrophy.
    Trüeb RM, Panizzon RG, Burg G.
    Dermatology; 1993 Jun; 186(3):205-9. PubMed ID: 8453149
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  • 3. Acrophobia in a Young Girl with Parathyroid Hormone Resistance (Pseudohypoparathyroidism).
    Gilani M, Memon AA, Asif N, Basharat N.
    J Coll Physicians Surg Pak; 2018 Sep; 28(9):S166-S168. PubMed ID: 30173686
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  • 4. Osteoma cutis and Albright's hereditary osteodystrophy.
    Brook CG, Valman HB.
    Br J Dermatol; 1971 Nov; 85(5):471-5. PubMed ID: 5002319
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  • 8. 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 Nov; 53(9):979-86. PubMed ID: 24785890
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  • 11. Molecular diagnosis and clinical characterization of pseudohypoparathyroidism type-Ib in a patient with mild Albright's hereditary osteodystrophy-like features, epileptic seizures, and defective renal handling of uric acid.
    Unluturk U, Harmanci A, Babaoglu M, Yasar U, Varli K, Bastepe M, Bayraktar M.
    Am J Med Sci; 2008 Jul; 336(1):84-90. PubMed ID: 18626245
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  • 12. Pseudohypoparathyroidism type 1b with hypothyroidism.
    Joshi R, Kapdi M.
    Indian Pediatr; 2012 Aug; 49(8):667-8. PubMed ID: 22962241
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  • 13. Albright's hereditary osteodystrophy.
    Wilson LC.
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():671-3. PubMed ID: 16789633
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  • 14. 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 15; 9(5):. PubMed ID: 35626900
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  • 19. Pseudohypoparathyroidism type 1B - a rare cause of tetany: case report.
    Garcia C, Correia CR, Lopes L.
    Paediatr Int Child Health; 2018 Nov 15; 38(4):281-284. PubMed ID: 28648114
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  • 20. [Albright's hereditary osteodystrophy: a case study].
    Tami L, Rherib C, Chefchaouni K, Knouni H, Barkat A.
    Pan Afr Med J; 2019 Nov 15; 34():190. PubMed ID: 32180864
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