Cano A - Search Results

1

Chabrol B, Mansour H, Cano A. Chabrol B, et al. Among authors: cano a. Presse Med. 2007 Mar;36 Spec No 1:1S32-5. Presse Med. 2007. PMID: 17546765 Review. French.

2

Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.

Giuliano F, Bannwarth S, Monnot S, Cano A, Chabrol B, Vialettes B, Delobel B, Paquis-Flucklinger V; French Group of WS. Giuliano F, et al. Among authors: cano a. Hum Mutat. 2005 Jan;25(1):99-100. doi: 10.1002/humu.9300. Hum Mutat. 2005. PMID: 15605410

3

[Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene].

Monnot S, Chabrol B, Cano A, Pellissier JF, Collignon P, Montfort MF, Paquis-Flucklinger V. Monnot S, et al. Among authors: cano a. Arch Pediatr. 2005 May;12(5):568-71. doi: 10.1016/j.arcped.2005.01.019. Arch Pediatr. 2005. PMID: 15885549 French.

4

[Metabolic diseases. Inherited metabolic diseases: importance of diagnosis].

Chabrol B, Cano A. Chabrol B, et al. Among authors: cano a. Ann Biol Clin (Paris). 2006 Nov-Dec;64(6):581-2. Ann Biol Clin (Paris). 2006. PMID: 17256234 Free article. French. No abstract available.

5

Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome.

Cano A, Rouzier C, Monnot S, Chabrol B, Conrath J, Lecomte P, Delobel B, Boileau P, Valero R, Procaccio V, Paquis-Flucklinger V; French Group of Wolfram Syndrome; Vialettes B. Cano A, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1605-12. doi: 10.1002/ajmg.a.31809. Am J Med Genet A. 2007. PMID: 17568405

6

Carnitine membrane transporter deficiency: a rare treatable cause of cardiomyopathy and anemia.

Cano A, Ovaert C, Vianey-Saban C, Chabrol B. Cano A, et al. Pediatr Cardiol. 2008 Jan;29(1):163-5. doi: 10.1007/s00246-007-9051-9. Epub 2007 Oct 10. Pediatr Cardiol. 2008. PMID: 17926086

7

Aortic dilatation in Cockayne syndrome.

Ovaert C, Cano A, Chabrol B. Ovaert C, et al. Among authors: cano a. Am J Med Genet A. 2007 Nov 1;143A(21):2604-6. doi: 10.1002/ajmg.a.31986. Am J Med Genet A. 2007. PMID: 17935247

8

Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome.

Chabrol B, Martens K, Meulemans S, Cano A, Jaeken J, Matthijs G, Creemers JW. Chabrol B, et al. Among authors: cano a. J Med Genet. 2008 May;45(5):314-8. doi: 10.1136/jmg.2007.055475. Epub 2008 Jan 30. J Med Genet. 2008. PMID: 18234729

9

[GLUT-1 deficiency syndrome or De Vivo disease: a case report].

Ticus I, Cano A, Villeneuve N, Milh M, Mancini J, Chabrol B. Ticus I, et al. Among authors: cano a. Arch Pediatr. 2008 Aug;15(8):1296-9. doi: 10.1016/j.arcped.2008.04.024. Epub 2008 Jun 16. Arch Pediatr. 2008. PMID: 18556184 French.

10

[Glucose transporter type 1 (GLUT-1) deficiency].

Cano A, Ticus I, Chabrol B. Cano A, et al. Rev Neurol (Paris). 2008 Nov;164(11):896-901. doi: 10.1016/j.neurol.2008.02.033. Epub 2008 Apr 3. Rev Neurol (Paris). 2008. PMID: 18808765 Review. French.

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