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 *

180 related articles for article (PubMed ID: 18520110)

  • 41. Genetic studies in a family with distal renal tubular acidosis and sensorineural deafness.
    Sethi SK; Singh N; Gil H; Bagga A
    Indian Pediatr; 2009 May; 46(5):425-7. PubMed ID: 19478356
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Progressive sensorineural hearing loss in association with distal renal tubular acidosis.
    Brown MT; Cunningham MJ; Ingelfinger JR; Becker AN
    Arch Otolaryngol Head Neck Surg; 1993 Apr; 119(4):458-60. PubMed ID: 8457310
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Incidence of radiographically evident bone disease, nephrocalcinosis, and nephrolithiasis in various types of renal tubular acidosis.
    Brenner RJ; Spring DB; Sebastian A; McSherry EM; Genant HK; Palubinskas AJ; Morris RC
    N Engl J Med; 1982 Jul; 307(4):217-21. PubMed ID: 7088070
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome.
    Fujimoto S; Yokochi K; Morikawa H; Nakano M; Shibata H; Togari H; Wada Y
    Am J Med Genet; 1999 Oct; 86(5):427-9. PubMed ID: 10508983
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene.
    Boualla L; Jdioui W; Soulami K; Ratbi I; Sefiani A
    Curr Res Transl Med; 2016; 64(1):5-8. PubMed ID: 27140593
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Clinical Auditory Phenotypes Associated with
    Wang L; Lin QF; Wang HY; Guan J; Lan L; Xie LY; Yu L; Yang J; Zhao C; Liang JL; Zhou HL; Yang HM; Xiong WP; Zhang QJ; Wang DY; Wang QJ
    Chin Med J (Engl); 2017 Mar; 130(6):703-709. PubMed ID: 28303854
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Medullary nephrocalcinosis, distal renal tubular acidosis and polycythaemia in a patient with nephrotic syndrome.
    Karunarathne S; Udayakumara Y; Govindapala D; Fernando H
    BMC Nephrol; 2012 Jul; 13():66. PubMed ID: 22834973
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome.
    Okawa T; Yoshida M; Usui T; Kudou T; Iwasaki Y; Fukuoka K; Takahashi N; Uehara Y; Oiso Y
    BMC Endocr Disord; 2015 Oct; 15():66. PubMed ID: 26514990
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A case of incomplete renal tubular acidosis (type 1) associated with medullary sponge kidney followed by nephrocalcinosis.
    Kumagai I; Matsuo S; Kato T
    J Urol; 1980 Feb; 123(2):250-2. PubMed ID: 7354533
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).
    Adachi M; Tachibana K; Asakura Y; Tsuchiya T
    J Pediatr Endocrinol Metab; 2006 Jan; 19(1):87-92. PubMed ID: 16509533
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome.
    Yeşiltepe Mutlu G; Kırmızıbekmez H; Nakamura A; Fukami M; Hatun Ş
    J Clin Res Pediatr Endocrinol; 2015 Dec; 7(4):344-8. PubMed ID: 26777049
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Renal tubular acidosis and sensorineural deafness: an autosomal recessive syndrome.
    Cremers CW; Monnens LA; Marres EH
    Arch Otolaryngol; 1980 May; 106(5):287-9. PubMed ID: 6768350
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Hereditary distal renal tubular acidosis: new understandings.
    Batlle D; Ghanekar H; Jain S; Mitra A
    Annu Rev Med; 2001; 52():471-84. PubMed ID: 11160790
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Persistent open anterior fontanel in a patient with distal renal tubular acidosis.
    Watanabe T; Yamazaki S; Nagayama Y
    Eur J Pediatr; 2007 Aug; 166(8):865-6. PubMed ID: 17043840
    [No Abstract]   [Full Text] [Related]  

  • 55. The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.
    Palazzo V; Provenzano A; Becherucci F; Sansavini G; Mazzinghi B; Orlandini V; Giunti L; Roperto RM; Pantaleo M; Artuso R; Andreucci E; Bargiacchi S; Traficante G; Stagi S; Murer L; Benetti E; Emma F; Giordano M; Rivieri F; Colussi G; Penco S; Manfredini E; Caruso MR; Garavelli L; Andrulli S; Vergine G; Miglietti N; Mancini E; Malaventura C; Percesepe A; Grosso E; Materassi M; Romagnani P; Giglio S
    Kidney Int; 2017 May; 91(5):1243-1255. PubMed ID: 28233610
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Distal tubular renal acidosis with nephrocalcinosis].
    Campoy Martínez P; Arrabal Martín M; Reina Ruiz C; Salazar Murillo R; Camacho Martínez E; Vilches Cocovi E; García Pérez M
    Actas Urol Esp; 1992 Apr; 16(4):338-40. PubMed ID: 1636459
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Bilateral Nephrocalcinosis in Primary Distal Renal Tubular Acidosis.
    Pitukweerakul S; Prachuapthunyachart S
    J Gen Intern Med; 2016 Oct; 31(10):1261. PubMed ID: 27090423
    [No Abstract]   [Full Text] [Related]  

  • 58. Distal renal tubular acidosis and lymphocytic thyroiditis with spontaneously resolving hyperthyroidism. Report of 1 case without nephrocalcinosis.
    Jaeger P; Portmann L; Wauters JP; Hürlimann J; Bill G; Scazziga B; Burckhardt P
    Am J Nephrol; 1985; 5(2):116-20. PubMed ID: 3838855
    [TBL] [Abstract][Full Text] [Related]  

  • 59. An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.
    Lichtner P; König R; Hasegawa T; Van Esch H; Meitinger T; Schuffenhauer S
    J Med Genet; 2000 Jan; 37(1):33-7. PubMed ID: 10633131
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Congenital absence of the parathyroid and thymus glands in an infant. (3 and 4 pharyngeal pouch syndrome).
    Taitz LS; Zarate-Salvador C; Schwartz E
    Pediatrics; 1966 Sep; 38(3):412-8. PubMed ID: 5950593
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.