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 *

119 related articles for article (PubMed ID: 7752494)

  • 1. [Idiopathic hypoparathyroidism (isolated)].
    Furukawa Y; Mizunashi K
    Nihon Rinsho; 1995 Apr; 53(4):968-73. PubMed ID: 7752494
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epilepsy and genetic malformations of the cerebral cortex.
    Guerrini R; Carrozzo R
    Am J Med Genet; 2001; 106(2):160-73. PubMed ID: 11579436
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism.
    Canaff L; Zhou X; Mosesova I; Cole DE; Hendy GN
    Hum Mutat; 2009 Jan; 30(1):85-92. PubMed ID: 18712808
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism.
    Bowl MR; Mirczuk SM; Grigorieva IV; Piret SE; Cranston T; Southam L; Allgrove J; Bahl S; Brain C; Loughlin J; Mughal Z; Ryan F; Shaw N; Thakker YV; Tiosano D; Nesbit MA; Thakker RV
    Hum Mol Genet; 2010 May; 19(10):2028-38. PubMed ID: 20190276
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy.
    Dahlberg PJ; Borer WZ; Newcomer KL; Yutuc WR
    Am J Med Genet; 1983 Sep; 16(1):99-104. PubMed ID: 6638075
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial isolated hypoparathyroidism: a molecular genetic analysis of 8 families with 23 affected persons.
    Ahn TG; Antonarakis SE; Kronenberg HM; Igarashi T; Levine MA
    Medicine (Baltimore); 1986 Mar; 65(2):73-81. PubMed ID: 3005800
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hypoparathyroidism associated with autoimmune disorder].
    Yamauchi M; Sugimoto T
    Clin Calcium; 2007 Aug; 17(8):1193-9. PubMed ID: 17660615
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Case of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome associated with nephrocalcinosis and distal renal tubular acidosis.
    Kato Y; Wada N; Numata A; Kakizaki H
    Int J Urol; 2007 May; 14(5):440-2. PubMed ID: 17511729
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Fabry's disease and hypoparathyroidism].
    Misery L; Gregoire M; Prieur F; Froissart R; Guffon N; Maitre S; Fond L; Denis L; Perrot JL; Cambazard F
    Ann Med Interne (Paris); 2002 Jun; 153(4):283-5. PubMed ID: 12218896
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The monogenic primary dystonias.
    Müller U
    Brain; 2009 Aug; 132(Pt 8):2005-25. PubMed ID: 19578124
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Classification of Hypoparathyroid Disorders.
    Cianferotti L
    Front Horm Res; 2019; 51():127-138. PubMed ID: 30641517
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Polyglandular autoimmune syndrome].
    Inaba M; Morii H
    Nihon Rinsho; 1995 Apr; 53(4):974-8. PubMed ID: 7752495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.
    Longo I; Scala E; Mari F; Caselli R; Pescucci C; Mencarelli MA; Speciale C; Giani M; Bresin E; Caringella DA; Borochowitz ZU; Siriwardena K; Winship I; Renieri A; Meloni I
    Nephrol Dial Transplant; 2006 Mar; 21(3):665-71. PubMed ID: 16338941
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Idiopathic hypoparathyroidism due to abnormalities in parathyroid organogenesis].
    Tanaka H
    Clin Calcium; 2007 Aug; 17(8):1206-13. PubMed ID: 17660617
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of AP2S1, a calcium-sensing receptor regulator, in familial and sporadic isolated hypoparathyroidism.
    Lambert AS; Grybek V; Francou B; Esterle L; Bertrand G; Bouligand J; Guiochon-Mantel A; Hieronimus S; Voitel D; Soskin S; Magdelaine C; Lienhardt A; Silve C; Linglart A
    J Clin Endocrinol Metab; 2014 Mar; 99(3):E469-73. PubMed ID: 24423332
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic malformations of the cerebral cortex and epilepsy.
    Guerrini R
    Epilepsia; 2005; 46 Suppl 1():32-7. PubMed ID: 15816977
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.
    Parvari R; Hershkovitz E; Grossman N; Gorodischer R; Loeys B; Zecic A; Mortier G; Gregory S; Sharony R; Kambouris M; Sakati N; Meyer BF; Al Aqeel AI; Al Humaidan AK; Al Zanhrani F; Al Swaid A; Al Othman J; Diaz GA; Weiner R; Khan KT; Gordon R; Gelb BD;
    Nat Genet; 2002 Nov; 32(3):448-52. PubMed ID: 12389028
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical and genetic features of the Alport 'syndromes'].
    Pescucci C; Longo I; Mari F; Scala E; Bruttini M; Caselli R; Renieri A
    G Ital Nefrol; 2005; 22(5):466-76. PubMed ID: 16267804
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 6.