Cano A - Search Results

1

Efficacy and safety of i.v. sodium benzoate in urea cycle disorders: a multicentre retrospective study.

Husson MC, Schiff M, Fouilhoux A, Cano A, Dobbelaere D, Brassier A, Mention K, Arnoux JB, Feillet F, Chabrol B, Guffon N, Elie C, de Lonlay P. Husson MC, et al. Among authors: cano a. Orphanet J Rare Dis. 2016 Sep 23;11(1):127. doi: 10.1186/s13023-016-0513-0. Orphanet J Rare Dis. 2016. PMID: 27663197 Free PMC article.

2

[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.

3

[Fabry disease in childhood].

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.

4

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

5

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

6

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

7

[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.

8

[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.

9

Multiple distal pulmonary arterial thromboses revealed by lung scintigraphy in a patient with homocystinuria and normal multidetector CT pulmonary angiography.

Tessonnier L, Guedj E, Cano A, Cammilleri S, Dragulescu A, Chabrol B, Mundler O. Tessonnier L, et al. Among authors: cano a. Clin Nucl Med. 2009 Jan;34(1):42-3. doi: 10.1097/RLU.0b013e31818f459a. Clin Nucl Med. 2009. PMID: 19092386 No abstract available.

10

Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency.

Boutron A, Acquaviva C, Vianey-Saban C, de Lonlay P, de Baulny HO, Guffon N, Dobbelaere D, Feillet F, Labarthe F, Lamireau D, Cano A, de Villemeur TB, Munnich A, Saudubray JM, Rabier D, Rigal O, Brivet M. Boutron A, et al. Among authors: cano a. Mol Genet Metab. 2011 Aug;103(4):341-8. doi: 10.1016/j.ymgme.2011.04.006. Epub 2011 Apr 19. Mol Genet Metab. 2011. PMID: 21549624

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