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Items: 1 to 20 of 83

1.

Congenital myotonic dystrophy: Canadian population-based surveillance study.

Campbell C, Levin S, Siu VM, Venance S, Jacob P.

J Pediatr. 2013 Jul;163(1):120-5.e1-3. doi: 10.1016/j.jpeds.2012.12.070. Epub 2013 Feb 14.

PMID:
23415617
2.

Congenital myotonic dystrophy: assisted ventilation duration and outcome.

Campbell C, Sherlock R, Jacob P, Blayney M.

Pediatrics. 2004 Apr;113(4):811-6.

PMID:
15060232
4.

Incidence of Smith-Lemli-Opitz syndrome in Canada: results of three-year population surveillance.

Nowaczyk MJ, Zeesman S, Waye JS, Douketis JD.

J Pediatr. 2004 Oct;145(4):530-5.

PMID:
15480380
5.

Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.

Zeesman S, Carson N, Whelan DT.

Am J Med Genet. 2002 Jan 22;107(3):222-6. Review.

PMID:
11807903
6.

Vitamin D-deficiency rickets among children in Canada.

Ward LM, Gaboury I, Ladhani M, Zlotkin S.

CMAJ. 2007 Jul 17;177(2):161-6. Epub 2007 Jun 28.

7.

[Spreading of the gene for myotonic dystrophy in Saguenay (Quebec)].

Bouchard G, Roy R, Declos M, Kouladjian K, Mathieu J.

J Genet Hum. 1988 Jun;36(3):221-37. French.

PMID:
3411303
8.

Cardiac involvement in myotonic dystrophy: a nationwide cohort study.

Lund M, Diaz LJ, Ranthe MF, Petri H, Duno M, Juncker I, Eiberg H, Vissing J, Bundgaard H, Wohlfahrt J, Melbye M.

Eur Heart J. 2014 Aug 21;35(32):2158-64. doi: 10.1093/eurheartj/ehu157. Epub 2014 Apr 16.

PMID:
24742887
9.

Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional study.

Johnson NE, Butterfield R, Berggren K, Hung M, Chen W, DiBella D, Dixon M, Hayes H, Pucillo E, Bounsanga J, Heatwole C, Campbell C.

Neurology. 2016 Jul 12;87(2):160-7. doi: 10.1212/WNL.0000000000002845. Epub 2016 Jun 15.

10.

Head injury secondary to suspected child maltreatment: results of a prospective Canadian national surveillance program.

Bennett S, Ward M, Moreau K, Fortin G, King J, Mackay M, Plint A.

Child Abuse Negl. 2011 Nov;35(11):930-6. doi: 10.1016/j.chiabu.2011.05.018. Epub 2011 Nov 17.

PMID:
22099143
11.

Epidemiological surveillance of myotonic dystrophy type 1: a 25-year population-based study.

Mathieu J, Prévost C.

Neuromuscul Disord. 2012 Nov;22(11):974-9. doi: 10.1016/j.nmd.2012.05.017. Epub 2012 Aug 1.

PMID:
22858159
12.

Congenital myotonic dystrophy in a national registry.

Prendergast P, Magalhaes S, Campbell C.

Paediatr Child Health. 2010 Oct;15(8):514-8.

14.

[Epidemiological study of Steinert's congenital myotonic dystrophy: dysmorphological characteristics].

González de Dios J, Martínez Frías ML, Egües Jimeno J, Gairi Tahull JM, Gómez Sabrido F, Morales Fernández MC, Paisán Grisolía L, Pardo Romero M, Medina Rams M.

An Esp Pediatr. 1999 Oct;51(4):389-96. Spanish.

PMID:
10690232
15.

The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects.

Reardon W, Newcombe R, Fenton I, Sibert J, Harper PS.

Arch Dis Child. 1993 Feb;68(2):177-81.

16.

Developmental Milestones and Quality of Life Assessment in a Congenital Myotonic Dystrophy Cohort.

Prasad M, Hicks R, MacKay M, Nguyen CT, Campbell C.

J Neuromuscul Dis. 2016 Aug 30;3(3):405-412.

PMID:
27854230
17.

The CNDR: collaborating to translate new therapies for Canadians.

Korngut L, Campbell C, Johnston M, Benstead T, Genge A, Mackenzie A, McCormick A, Biggar D, Bourque P, Briemberg H, O'Connell C, Dojeiji S, Dooley J, Grant I, Hogan G, Johnston W, Kalra S, Katzberg HD, Mah JK, McAdam L, McMillan HJ, Melanson M, Selby K, Shoesmith C, Smith G, Venance SL, Wee J; CNDR Investigator Network.

Can J Neurol Sci. 2013 Sep;40(5):698-704.

PMID:
23968944
18.

Infant mortality in myotonic dystrophy in Saguenay-Lac-St-Jean: a historical perspective.

Dao TN, Mathieu J, Bouchard JP, De Braekeleer M.

Clin Genet. 1993 Jan;43(1):25-7.

PMID:
8462193
19.

Successful use of BiPAP in infants with congenital myotonic dystrophy.

Chau SK, Lee SL.

Pediatr Int. 2013 Apr;55(2):243-5. doi: 10.1111/j.1442-200X.2012.03732.x.

PMID:
23679166
20.

Age and causes of death in adult-onset myotonic dystrophy.

de Die-Smulders CE, Höweler CJ, Thijs C, Mirandolle JF, Anten HB, Smeets HJ, Chandler KE, Geraedts JP.

Brain. 1998 Aug;121 ( Pt 8):1557-63.

PMID:
9712016

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