Bernard C - Search Results

1

Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol.

Lee CY, Krimbou L, Vincent J, Bernard C, Larramée P, Genest J Jr, Marcil M. Lee CY, et al. Among authors: bernard c. Hum Genet. 2003 May;112(5-6):552-62. doi: 10.1007/s00439-002-0893-1. Epub 2003 Feb 27. Hum Genet. 2003. PMID: 12607113

2

ARHGDIA: a novel gene implicated in nephrotic syndrome.

Gupta IR, Baldwin C, Auguste D, Ha KC, El Andalousi J, Fahiminiya S, Bitzan M, Bernard C, Akbari MR, Narod SA, Rosenblatt DS, Majewski J, Takano T. Gupta IR, et al. Among authors: bernard c. J Med Genet. 2013 May;50(5):330-8. doi: 10.1136/jmedgenet-2012-101442. Epub 2013 Feb 22. J Med Genet. 2013. PMID: 23434736 Free PMC article.

3

Renal tubular dysgenesis and microcolon, a novel association. Report of three cases.

Saskin A, Alfares A, Bernard C, Blumenkrantz M, Braverman N, Gupta I, Brosnihan KB, Antignac C, Gubler MC, Morinière V, De Bie I, Bitzan M. Saskin A, et al. Among authors: bernard c. Eur J Med Genet. 2019 Apr;62(4):254-258. doi: 10.1016/j.ejmg.2018.07.024. Epub 2018 Jul 31. Eur J Med Genet. 2019. PMID: 30071301

4

Cardiac pathology in sudden unexpected infant death.

Dancea A, Côté A, Rohlicek C, Bernard C, Oligny LL. Dancea A, et al. Among authors: bernard c. J Pediatr. 2002 Sep;141(3):336-42. doi: 10.1067/mpd.2002.126340. J Pediatr. 2002. PMID: 12219052

5

Acute tubular dysfunction with Fanconi syndrome: a new manifestation of mitochondrial cytopathies.

Debray FG, Merouani A, Lambert M, Brochu P, Bernard C, Robinson BH, Mitchell GA. Debray FG, et al. Among authors: bernard c. Am J Kidney Dis. 2008 Apr;51(4):691-6. doi: 10.1053/j.ajkd.2007.11.024. Am J Kidney Dis. 2008. PMID: 18371545 Free article. No abstract available.

6

Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome.

Mitchell J, Punthakee Z, Lo B, Bernard C, Chong K, Newman C, Cartier L, Desilets V, Cutz E, Hansen IL, Riley P, Polychronakos C. Mitchell J, et al. Among authors: bernard c. Diabetologia. 2004 Dec;47(12):2160-7. doi: 10.1007/s00125-004-1576-3. Epub 2004 Dec 8. Diabetologia. 2004. PMID: 15592663

7

Clinical features of X-linked nephrolithiasis in childhood.

Langlois V, Bernard C, Scheinman SJ, Thakker RV, Cox JP, Goodyer PR. Langlois V, et al. Among authors: bernard c. Pediatr Nephrol. 1998 Oct;12(8):625-9. doi: 10.1007/s004670050516. Pediatr Nephrol. 1998. PMID: 9811383

8

Sternocostoclavicular hyperostosis in children: a report of eight cases.

Azouz EM, Jurik AG, Bernard C. Azouz EM, et al. Among authors: bernard c. AJR Am J Roentgenol. 1998 Aug;171(2):461-6. doi: 10.2214/ajr.171.2.9694476. AJR Am J Roentgenol. 1998. PMID: 9694476

9

Foveolar hyperplasia secondary to cow's milk protein hypersensitivity presenting with clinical features of pyloric stenosis.

Morinville V, Bernard C, Forget S. Morinville V, et al. Among authors: bernard c. J Pediatr Surg. 2004 Jan;39(1):E29-31. doi: 10.1016/j.jpedsurg.2003.09.040. J Pediatr Surg. 2004. PMID: 14694404

10

Pericardial hemangioma presenting as thoracic mass in utero.

Puligandla PS, Kay S, Morin L, Desilets V, Jutras L, Shum-Tim D, Bernard C, Flageole H. Puligandla PS, et al. Among authors: bernard c. Fetal Diagn Ther. 2004 Mar-Apr;19(2):178-81. doi: 10.1159/000075146. Fetal Diagn Ther. 2004. PMID: 14764966

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