Prevalence and clinical correlates of CACNA1D mutations in primary aldosteronism

被引：0
|
作者：
Riester, A. [1 ]
Osswald, A. [1 ]
Fischer, E. [1 ]
Strom, T. M. [2 ]
Beuschlein, F. [1 ]
Reincke, M. [1 ]
机构：
[1] LMU Munchen, Med Klin & Poliklin 4, Munich, Germany
[2] Helmholtz Zentrum Munchen, Inst Human Genet, Munich, Germany
来源：
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES | 2014年 / 122卷 / 03期
关键词：
D O I：
10.1055/s-0034-1371995
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
OP5_20
引用
收藏
页数：2
相关论文
共 50 条
  • [41] The L-Type Calcium Channel Genes CACNA1C and CACNA1D Are Associated with Cellular Circadian Rhythm Abnormalities in Bipolar Disorder
    McCarthy, Michael
    Wei, Heather
    Le Roux, Melissa
    Kelsoe, John
    Welsh, David
    NEUROPSYCHOPHARMACOLOGY, 2014, 39 : S312 - S313
  • [42] Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness
    Shahid M Baig
    Alexandra Koschak
    Andreas Lieb
    Mathias Gebhart
    Claudia Dafinger
    Gudrun Nürnberg
    Amjad Ali
    Ilyas Ahmad
    Martina J Sinnegger-Brauns
    Niels Brandt
    Jutta Engel
    Matteo E Mangoni
    Muhammad Farooq
    Habib U Khan
    Peter Nürnberg
    Jörg Striessnig
    Hanno J Bolz
    Nature Neuroscience, 2011, 14 : 77 - 84
  • [43] CACNA1D overexpression and voltage-gated calcium channels in prostate cancer during androgen deprivation
    McKerr, Niamh
    Mohd-Sarip, Adone
    Dorrian, Hannah
    Breen, Conor
    A. James, Jacqueline
    McQuaid, Stephen
    Mills, Ian G.
    McCloskey, Karen D.
    SCIENTIFIC REPORTS, 2023, 13 (01)
  • [44] High prevalence of CACNA1A truncating mutations and broader clinical spectrum in episodic ataxia type 2
    Denier, C
    Ducros, A
    Joutel, A
    Vahedi, K
    Tournier-Lasserve, T
    NEUROLOGY, 1999, 52 (06) : A116 - A116
  • [45] Pregnancy, Primary Aldosteronism, and Adrenal CTNNB1 Mutations
    Teo, Ada E. D.
    Garg, Sumedha
    Shaikh, Lalarukh Haris
    Zhou, Junhua
    Frankl, Fiona E. Karet
    Gurnell, Mark
    Happerfield, Lisa
    Marker, Alison
    Bienz, Mariann
    Azizan, Elena A. B.
    Brown, Morris J.
    NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (15): : 1429 - 1436
  • [46] Pregnancy, Primary Aldosteronism, and Somatic CTNNB1 Mutations
    Berthon, Annabel
    Drelon, Coralie
    Val, Pierre
    NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (15): : 1493 - 1494
  • [47] Effects of Cacna1d D307G Mutation on Blood Pressure and Kidney Function in Rats with Salt Loading
    Cheng, Lan
    Chen, Hui
    Maboh, R. Nfornah
    Wang, Huan
    KIDNEY & BLOOD PRESSURE RESEARCH, 2025, 50 (01): : 46 - 60
  • [48] Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant
    Ezell, Kimberly M.
    Tinker, Rory J.
    Furuta, Yutaka
    Gulsevin, Alican
    Bastarache, Lisa
    Hamid, Rizwan
    Cogan, Joy D.
    Rives, Lynette
    Neumann, Serena
    Corner, Brian
    Kozuria, Mary
    Phillips, John A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2024, 194 (07)
  • [49] Clinical characteristics of primary aldosteronism: its prevalence and comparative studies on various causes of primary aldosteronism in Yokohama Rosai Hospital
    Nishikawa, T
    Omura, M
    BIOMEDICINE & PHARMACOTHERAPY, 2000, 54 : 83S - 85S
  • [50] CACNA1D overexpression and voltage-gated calcium channels in prostate cancer during androgen deprivation
    Niamh McKerr
    Adone Mohd-Sarip
    Hannah Dorrian
    Conor Breen
    Jacqueline A. James
    Stephen McQuaid
    Ian G. Mills
    Karen D. McCloskey
    Scientific Reports, 13
12345