Blaichman S - Search Results

1

Treatment of familial hypercholesterolemia in children and adolescents: effect of lovastatin. Canadian Lovastatin in Children Study Group.

Lambert M, Lupien PJ, Gagné C, Lévy E, Blaichman S, Langlois S, Hayden M, Rose V, Clarke JT, Wolfe BM, Clarson C, Parsons H, Stephure DK, Potvin D, Lambert J. Lambert M, et al. Among authors: blaichman s. Pediatrics. 1996 May;97(5):619-28. Pediatrics. 1996. PMID: 8628597 Clinical Trial.

2

Homozygous familial hypercholesterolemia among French Canadians in Québec Province.

Moorjani S, Roy M, Gagné C, Davignon J, Brun D, Toussaint M, Lambert M, Campeau L, Blaichman S, Lupien P. Moorjani S, et al. Among authors: blaichman s. Arteriosclerosis. 1989 Mar-Apr;9(2):211-6. doi: 10.1161/01.atv.9.2.211. Arteriosclerosis. 1989. PMID: 2923577

3

Geographic distribution of French-Canadian low-density lipoprotein receptor gene mutations in the Province of Quebec.

Vohl MC, Moorjani S, Roy M, Gaudet D, Torres AL, Minnich A, Gagné C, Tremblay G, Lambert M, Bergeron J, Couture P, Perron P, Blaichman S, Brun LD, Davignon J, Lupien PJ, Després JP. Vohl MC, et al. Among authors: blaichman s. Clin Genet. 1997 Jul;52(1):1-6. doi: 10.1111/j.1399-0004.1997.tb02506.x. Clin Genet. 1997. PMID: 9272705

4

Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans.

Treacy E, Polychronakos C, Vekemans M, Eydoux P, Blaichman S, Scarpelli H, Ross M, Xu Y, Der Kaloustian VM. Treacy E, et al. Among authors: blaichman s. J Med Genet. 1996 Jan;33(1):42-6. doi: 10.1136/jmg.33.1.42. J Med Genet. 1996. PMID: 8825047 Free PMC article.

5

Syndrome of mental retardation and distal arthrogryposis in sibs.

Chitayat D, Hodgkinson KA, Blaichman S, Chen ME, Watters GV, Khalife S, Hall JG. Chitayat D, et al. Among authors: blaichman s. Am J Med Genet. 1991 Oct 1;41(1):49-51. doi: 10.1002/ajmg.1320410114. Am J Med Genet. 1991. PMID: 1951463

6

Costello syndrome.

Der Kaloustian VM, Moroz B, McIntosh N, Watters AK, Blaichman S. Der Kaloustian VM, et al. Among authors: blaichman s. Am J Med Genet. 1991 Oct 1;41(1):69-73. doi: 10.1002/ajmg.1320410118. Am J Med Genet. 1991. PMID: 1951465

7

Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: a new syndrome.

Der Kaloustian VM, McIntosh N, Silver K, Blaichman S, Halal F. Der Kaloustian VM, et al. Among authors: blaichman s. Am J Med Genet. 1992 Aug 1;43(6):942-5. doi: 10.1002/ajmg.1320430607. Am J Med Genet. 1992. PMID: 1384331

8

Tracheoesophageal fistula, protruding pinnae, proximal interphalangeal symphalangism of fifth finger. A new syndrome?

Blaichman S. Blaichman S. Am J Med Genet. 1982 Oct;13(2):233-4. doi: 10.1002/ajmg.1320130215. Am J Med Genet. 1982. PMID: 7137234 No abstract available.

9

Advocacy and compliance in genetic screening. Behavior of physicians and clients in a voluntary program of testing for the Tay-Sachs gene.

Beck E, Blaichman S, Scriver CR, Clow CL. Beck E, et al. Among authors: blaichman s. N Engl J Med. 1974 Nov 28;291(22):1166-70. doi: 10.1056/NEJM197411282912206. N Engl J Med. 1974. PMID: 4418237 No abstract available.

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