This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 1927 Mar 19;1(3454):504-6.

doi: 10.1136/bmj.1.3454.504.

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS

PMID: 20773074
PMCID: PMC2454341
DOI: 10.1136/bmj.1.3454.504

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS

A C Alport. Br Med J. 1927.

. 1927 Mar 19;1(3454):504-6.

doi: 10.1136/bmj.1.3454.504.

Author

PMID: 20773074
PMCID: PMC2454341
DOI: 10.1136/bmj.1.3454.504

No abstract available

PubMed Disclaimer

Similar articles

Nonfamilial hematuria associated with glomerular basement membrane alterations characteristic of hereditary nephritis: comparison with hereditary nephritis.
Yoshikawa N, Matsuyama S, Ito H, Hajikano H, Matsuo T. Yoshikawa N, et al. J Pediatr. 1987 Oct;111(4):519-24. doi: 10.1016/s0022-3476(87)80111-7. J Pediatr. 1987. PMID: 3655982
[Dysembryogenesis in hereditary nephritis].
Ignatova MS, Degtiareva EM, Fokeeva VV, Skripkina LA. Ignatova MS, et al. Genetika. 1975;11(11):114-20. Genetika. 1975. PMID: 1228057 Russian.
Hereditary nephritis associated with vesicoureteral reflux and vaginal duplication.
Bissada NK, Redman JF. Bissada NK, et al. Urology. 1976 Apr;7(4):409-11. doi: 10.1016/0090-4295(76)90257-0. Urology. 1976. PMID: 1265947
Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia.
Vorselaars VMM, Hosman AE, Westermann CJJ, Snijder RJ, Mager JJ, Goumans MJ, Post MC. Vorselaars VMM, et al. Int J Mol Sci. 2018 Oct 17;19(10):3203. doi: 10.3390/ijms19103203. Int J Mol Sci. 2018. PMID: 30336550 Free PMC article. Review.
[Sibling cases of nephritis resembling membranoproliferative glomerulonephritis].
Ueda H, Isimura E, Okuno S, Maekawa K, Izumotani T, Kim M, Matsumoto N, Fukumoto S, Imanishi Y, Emoto M, Shoji T, Wanibuchi H, Inaba M, Nishizawa Y. Ueda H, et al. Nihon Jinzo Gakkai Shi. 2002 May;44(4):420-6. Nihon Jinzo Gakkai Shi. 2002. PMID: 12073629 Review. Japanese.

See all similar articles

Cited by

Alport Syndrome: De Novo Mutation in the COL4A5 Gene Converting Glycine 1205 to Valine.
Antón-Martín P, Aparicio López C, Ramiro-León S, Santillán Garzón S, Santos-Simarro F, Gil-Fournier B. Antón-Martín P, et al. Clin Med Insights Pediatr. 2012 Jun 28;6:41-9. doi: 10.2147/CBF.S23366. Print 2012. Clin Med Insights Pediatr. 2012. PMID: 23641165 Free PMC article.
Alport's Syndrome in Pregnancy.
Mehta S, Saifan C, Abdellah M, Choueiry R, Nasr R, El-Sayegh S. Mehta S, et al. Case Rep Med. 2013;2013:374020. doi: 10.1155/2013/374020. Epub 2013 Jun 3. Case Rep Med. 2013. PMID: 23861686 Free PMC article.
A Novel Mutation in a Kazakh Family with X-Linked Alport Syndrome.
Baikara BT, Zholdybayeva EV, Rakhimova SE, Nigmatullina NB, Momynaliev KT, Ramanculov YM. Baikara BT, et al. PLoS One. 2015 Jul 13;10(7):e0132010. doi: 10.1371/journal.pone.0132010. eCollection 2015. PLoS One. 2015. PMID: 26168235 Free PMC article.
Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation.
Iijima K, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M. Iijima K, et al. Pediatr Nephrol. 2010 Oct;25(10):2165-70. doi: 10.1007/s00467-010-1514-1. Epub 2010 Apr 13. Pediatr Nephrol. 2010. PMID: 20386926
[Analysis of Alport syndrome induced by type IV collagen alpha 5 gene mutation in two families].
Ye Q, Zhang Y, Wang J, Mao J. Ye Q, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):384-389. doi: 10.3785/j.issn.1008-9292.2019.08.06. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019. PMID: 31901041 Free PMC article. Chinese.

See all "Cited by" articles

LinkOut - more resources

Full Text Sources
- Europe PubMed Central
- PubMed Central