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Journal Abstract Search


126 related items for PubMed ID: 29429567

  • 1. Pseudopseudohypoparathyroidism: A Diagnostic Consideration in a Patient with Brachydactyly.
    Benvenuto P, Attarian A.
    J Pediatr; 2018 May; 196():321. PubMed ID: 29429567
    [No Abstract] [Full Text] [Related]

  • 2. A Case of Soft Tissue Ossifications: A Case Report.
    Arrigoni P, Minen A.
    JBJS Case Connect; 2019 May; 9(2):e0287. PubMed ID: 31085937
    [Abstract] [Full Text] [Related]

  • 3. [GNAS1 gene abnormality in pseudohypoparathyroidism I a].
    Ozono K.
    Clin Calcium; 2007 Aug; 17(8):1214-9. PubMed ID: 17660618
    [Abstract] [Full Text] [Related]

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  • 6. [Pseudoidiopathic hypoparathyroidism and pseudopseudohypoparathyroidism].
    Okazaki R.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():66-9. PubMed ID: 16817352
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  • 9. Pseudopseudohypoparathyroidism.
    Simpson C, Grove E, Houston BA.
    Lancet; 2015 Mar 21; 385(9973):1123. PubMed ID: 25484027
    [No Abstract] [Full Text] [Related]

  • 10. Albright's hereditary osteodystrophy and pseudohypoparathyroidism.
    Wilson LC, Hall CM.
    Semin Musculoskelet Radiol; 2002 Dec 21; 6(4):273-83. PubMed ID: 12541184
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  • 12. Albright's hereditary osteodystrophy.
    Kapoor S, Gogia S, Paul R, Banerjee S.
    Indian J Pediatr; 2006 Feb 21; 73(2):153-6. PubMed ID: 16514227
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  • 13. Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1.
    Garavelli L, Pedori S, Zanacca C, Caselli G, Loiodice A, Mantovani G, Ammenti A, Virdis R, Banchini G.
    Acta Biomed; 2005 Apr 21; 76(1):45-8. PubMed ID: 16116826
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  • 15. [Albright hereditary osteodystrophy: identification of a novel mutation in a family].
    Bastida Eizaguirre M, Iturbe Ortiz De Urbina R, Arto Urzainqui M, Ezquerra Larreina R, Escalada San Martín J.
    An Esp Pediatr; 2001 Jun 21; 54(6):598-600. PubMed ID: 11412411
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  • 17. Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.
    Levine MA, Jap TS, Mauseth RS, Downs RW, Spiegel AM.
    J Clin Endocrinol Metab; 1986 Mar 21; 62(3):497-502. PubMed ID: 3003142
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  • 18. Albright's hereditary osteodystrophy (pseudohypoparathyroidism or pseudo-pseudohypoparathyroidism).
    Blizzard RM, Temtamy S, Steinhauser RA, Char F.
    Birth Defects Orig Artic Ser; 1971 May 21; 7(6):268-74. PubMed ID: 5173177
    [No Abstract] [Full Text] [Related]

  • 19. Brachydactyly in 14 genetically characterized pseudohypoparathyroidism type Ia patients.
    de Sanctis L, Vai S, Andreo MR, Romagnolo D, Silvestro L, de Sanctis C.
    J Clin Endocrinol Metab; 2004 Apr 21; 89(4):1650-5. PubMed ID: 15070926
    [Abstract] [Full Text] [Related]

  • 20. [Pseudopseudohypoparathyroidism and genomic imprinting].
    Minagawa M.
    Clin Calcium; 2007 Aug 21; 17(8):1229-33. PubMed ID: 17660620
    [Abstract] [Full Text] [Related]


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