Ronco P - Search Results

1

Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome.

Alamowitch S, Plaisier E, Favrole P, Prost C, Chen Z, Van Agtmael T, Marro B, Ronco P. Alamowitch S, et al. Among authors: ronco p. Neurology. 2009 Dec 1;73(22):1873-82. doi: 10.1212/WNL.0b013e3181c3fd12. Neurology. 2009. PMID: 19949034 Free PMC article.

2

COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps.

Plaisier E, Gribouval O, Alamowitch S, Mougenot B, Prost C, Verpont MC, Marro B, Desmettre T, Cohen SY, Roullet E, Dracon M, Fardeau M, Van Agtmael T, Kerjaschki D, Antignac C, Ronco P. Plaisier E, et al. Among authors: ronco p. N Engl J Med. 2007 Dec 27;357(26):2687-95. doi: 10.1056/NEJMoa071906. N Engl J Med. 2007. PMID: 18160688 Free article.

3

[HANAC syndrome (hereditary angiopathy with nephropathy, aneurysms and muscle cramps) and mutations of the collagen 4A1 gene: a new basement membrane hereditary pathology with multisystemic expression].

Plaisier E, Ronco P. Plaisier E, et al. Among authors: ronco p. Nephrol Ther. 2008 Dec;4(7):632-4. doi: 10.1016/j.nephro.2008.03.013. Epub 2008 Sep 24. Nephrol Ther. 2008. PMID: 18818132 French. No abstract available.

4

[Hereditary angiopathy with nephropathy, aneurysms and muscle cramps (HANAC): a new basement membrane-disease associated with mutations of the COL4A1 gene].

Ronco P, Plaisier E. Ronco P, et al. Bull Acad Natl Med. 2008 May;192(5):971-84; discussion 984-6. Bull Acad Natl Med. 2008. PMID: 19238787 French.

5

Novel COL4A1 mutations associated with HANAC syndrome: a role for the triple helical CB3[IV] domain.

Plaisier E, Chen Z, Gekeler F, Benhassine S, Dahan K, Marro B, Alamowitch S, Paques M, Ronco P. Plaisier E, et al. Among authors: ronco p. Am J Med Genet A. 2010 Oct;152A(10):2550-5. doi: 10.1002/ajmg.a.33659. Am J Med Genet A. 2010. PMID: 20818663

6

HANAC Syndrome Col4a1 Mutation Causes Neonate Glomerular Hyperpermeability and Adult Glomerulocystic Kidney Disease.

Chen Z, Migeon T, Verpont MC, Zaidan M, Sado Y, Kerjaschki D, Ronco P, Plaisier E. Chen Z, et al. Among authors: ronco p. J Am Soc Nephrol. 2016 Apr;27(4):1042-54. doi: 10.1681/ASN.2014121217. Epub 2015 Aug 10. J Am Soc Nephrol. 2016. PMID: 26260163 Free PMC article.

7

Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: a novel syndrome.

Plaisier E, Alamowitch S, Gribouval O, Mougenot B, Gaudric A, Antignac C, Roullet E, Ronco P. Plaisier E, et al. Among authors: ronco p. Kidney Int. 2005 Jun;67(6):2354-60. doi: 10.1111/j.1523-1755.2005.00341.x. Kidney Int. 2005. PMID: 15882279 Free article.

8

HANAC Col4a1 Mutation in Mice Leads to Skeletal Muscle Alterations due to a Primary Vascular Defect.

Guiraud S, Migeon T, Ferry A, Chen Z, Ouchelouche S, Verpont MC, Sado Y, Allamand V, Ronco P, Plaisier E. Guiraud S, et al. Among authors: ronco p. Am J Pathol. 2017 Mar;187(3):505-516. doi: 10.1016/j.ajpath.2016.10.020. Epub 2017 Jan 3. Am J Pathol. 2017. PMID: 28056338 Free PMC article.

9

Col4a1 mutation generates vascular abnormalities correlated with neuronal damage in a mouse model of HANAC syndrome.

Trouillet A, Lorach H, Dubus E, El Mathari B, Ivkovic I, Dégardin J, Simonutti M, Paques M, Guillonneau X, Sennlaub F, Sahel JA, Ronco P, Plaisier E, Picaud S. Trouillet A, et al. Among authors: ronco p. Neurobiol Dis. 2017 Apr;100:52-61. doi: 10.1016/j.nbd.2016.12.014. Epub 2017 Jan 3. Neurobiol Dis. 2017. PMID: 28057519

10

Ig-related renal disease in lymphoplasmacytic disorders: an update.

Ronco P, Plaisier E, Aucouturier P. Ronco P, et al. Semin Nephrol. 2010 Nov;30(6):557-69. doi: 10.1016/j.semnephrol.2010.09.004. Semin Nephrol. 2010. PMID: 21146121 Review.

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