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 *

128 related articles for article (PubMed ID: 35948208)

  • 21. New peripapillary findings in Alport syndrome: A case report.
    Doménech-Aracil N; Hernández-Bel L; Castro-Navarro V; Barrios-Poleo C; Hernández Garfella M; Cervera-Taulet E
    Arch Soc Esp Oftalmol; 2015 Oct; 90(10):497-8. PubMed ID: 25443209
    [No Abstract]   [Full Text] [Related]  

  • 22. Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
    Chen Y; Colville D; Ierino F; Symons A; Savige J
    Ophthalmic Genet; 2018 Apr; 39(2):208-214. PubMed ID: 29172845
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms.
    Liu J; Colville D; Wang YY; Baird PN; Guymer RH; Savige J
    Br J Ophthalmol; 2009 Mar; 93(3):379-82. PubMed ID: 19019939
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Alport's syndrome and flecked retinopathy.
    Gelisken O; Ozçetin H; Erturk H
    Bull Soc Belge Ophtalmol; 1986; 220():75-9. PubMed ID: 3452470
    [No Abstract]   [Full Text] [Related]  

  • 25. Alport retinopathy results from "severe" COL4A5 mutations and predicts early renal failure.
    Tan R; Colville D; Wang YY; Rigby L; Savige J
    Clin J Am Soc Nephrol; 2010 Jan; 5(1):34-8. PubMed ID: 19965530
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Rare ocular manifestation with suspect alport syndrome].
    Krejčířová I; Varadyová B; Doležel Z; Autrata R; Matúšová J; Gregorová E
    Cesk Slov Oftalmol; 2014 Jun; 70(3):114-8. PubMed ID: 25032798
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Cone dystrophy associated with Alport syndrome].
    Spraul CW; Lang GE
    Klin Monbl Augenheilkd; 2000 Sep; 217(3):194-7. PubMed ID: 11076352
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Giant macular hole in Alport syndrome.
    Rahman W; Banerjee S
    Can J Ophthalmol; 2007 Apr; 42(2):314-5. PubMed ID: 17392861
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Esophageal leiomyomatosis revealing an Alport syndrome].
    Abbes K; Ayadi L; Makni S; Kharrat M; Affes N; Kallel R; Gouiaa N; Ben Hmida M; Hachicha J; Beyrouti MI; Sellami Boudawara T
    Rev Med Interne; 2009 Jan; 30(1):88-90. PubMed ID: 18433941
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Ocular manifestations of Alport's syndrome: a case report.
    Acke I; Priem H
    Bull Soc Belge Ophtalmol; 1992; 243():123-8. PubMed ID: 1302141
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A triad of retinal signs in Alport syndrome: The 'stair-case' fovea, choroidal thinning and peripheral schisis.
    Ghadiri NJ; Stanojcic N; Raja M; Burton BJ
    Eur J Ophthalmol; 2019 Jul; 29(1_suppl):10-14. PubMed ID: 30957516
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [A new case of giant macular hole in a patient with Alport syndrome].
    Mercé E; Korobelnik JF; Delyfer MN; Rougier MB
    J Fr Ophtalmol; 2012 Oct; 35(8):573-9. PubMed ID: 22695059
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Role of multimodal ocular imaging in Alport syndrome.
    Kapoor A; Kapoor S; Chawla R
    Can J Ophthalmol; 2022 Jun; 57(3):e77-e78. PubMed ID: 34324875
    [No Abstract]   [Full Text] [Related]  

  • 34. Ocular manifestations of autosomal recessive Alport syndrome.
    Colville D; Savige J; Morfis M; Ellis J; Kerr P; Agar J; Fasset R
    Ophthalmic Genet; 1997 Sep; 18(3):119-28. PubMed ID: 9361309
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Outcome of females with Alport syndrome.
    Koyun M; Aksoy GK; Çomak E; Akman S
    Pediatr Nephrol; 2022 Aug; 37(8):1937. PubMed ID: 35478268
    [No Abstract]   [Full Text] [Related]  

  • 36. Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
    Kamiyoshi N; Nozu K; Fu XJ; Morisada N; Nozu Y; Ye MJ; Imafuku A; Miura K; Yamamura T; Minamikawa S; Shono A; Ninchoji T; Morioka I; Nakanishi K; Yoshikawa N; Kaito H; Iijima K
    Clin J Am Soc Nephrol; 2016 Aug; 11(8):1441-1449. PubMed ID: 27281700
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Autosomal recessive Alport syndrome: mutation in the COL4A3 gene in a woman with Alport syndrome and posttransplant antiglomerular basement membrane nephritis.
    Ding J; Stitzel J; Berry P; Hawkins E; Kashtan CE
    J Am Soc Nephrol; 1995 Mar; 5(9):1714-7. PubMed ID: 7780062
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Alport Syndrome in Women and Girls.
    Savige J; Colville D; Rheault M; Gear S; Lennon R; Lagas S; Finlay M; Flinter F
    Clin J Am Soc Nephrol; 2016 Sep; 11(9):1713-1720. PubMed ID: 27287265
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.
    Antignac C; Heidet L
    Contrib Nephrol; 1996; 117():172-82. PubMed ID: 8801045
    [No Abstract]   [Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 7.