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Items: 1 to 50 of 133

1.

Wisdom: What is it?

Haworth JC.

Paediatr Child Health. 2012 Apr;17(4):179. No abstract available.

2.

Defects in DNA ligase I trigger PCNA ubiquitylation at Lys 107.

Das-Bradoo S, Nguyen HD, Wood JL, Ricke RM, Haworth JC, Bielinsky AK.

Nat Cell Biol. 2010 Jan;12(1):74-9; sup pp 1-20. doi: 10.1038/ncb2007. Epub 2009 Dec 13.

3.

The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations.

Greenberg CR, Dilling LA, Thompson GR, Seargeant LE, Haworth JC, Phillips S, Chan A, Vallance HD, Waters PJ, Sinclair G, Lillquist Y, Wanders RJ, Olpin SE.

Mol Genet Metab. 2009 Apr;96(4):201-7. doi: 10.1016/j.ymgme.2008.12.018. Epub 2009 Feb 13.

PMID:
19217814
4.

Congenital rickets caused by maternal vitamin D deficiency.

Innes AM, Seshia MM, Prasad C, Al Saif S, Friesen FR, Chudley AE, Reed M, Dilling LA, Haworth JC, Greenberg CR.

Paediatr Child Health. 2002 Sep;7(7):455-8.

5.

Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada.

Greenberg CR, Prasad AN, Dilling LA, Thompson JR, Haworth JC, Martin B, Wood-Steiman P, Seargeant LE, Seifert B, Booth FA, Prasad C.

Mol Genet Metab. 2002 Jan;75(1):70-8.

PMID:
11825066
6.

Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.

Holzinger A, Maier EM, Bück C, Mayerhofer PU, Kappler M, Haworth JC, Moroz SP, Hadorn HB, Sadler JE, Roscher AA.

Am J Hum Genet. 2002 Jan;70(1):20-5. Epub 2001 Nov 21.

7.

Celiac disease in a patient with a congenital deficiency of intestinal enteropeptidase.

Moroz SP, Hadorn B, Rossi TM, Haworth JC.

Am J Gastroenterol. 2001 Jul;96(7):2251-4.

PMID:
11467662
8.

Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program.

Prasad C, Johnson JP, Bonnefont JP, Dilling LA, Innes AM, Haworth JC, Beischel L, Thuillier L, Prip-Buus C, Singal R, Thompson JR, Prasad AN, Buist N, Greenberg CR.

Mol Genet Metab. 2001 May;73(1):55-63.

PMID:
11350183
9.

Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite community.

Prip-Buus C, Thuillier L, Abadi N, Prasad C, Dilling L, Klasing J, Demaugre F, Greenberg CR, Haworth JC, Droin V, Kadhom N, Gobin S, Kamoun P, Girard J, Bonnefont JP.

Mol Genet Metab. 2001 May;73(1):46-54.

PMID:
11350182
10.

Genetic landmarks through philately-hemophilia.

Chudley AE, Haworth JC.

Clin Genet. 1999 Oct;56(4):279-81. No abstract available.

PMID:
10636445
11.

Genetic landmarks through philately--porphyria and its effect on world history.

Chudley AE, Haworth JC.

Clin Genet. 1999 Feb;55(2):85-7. No abstract available.

PMID:
10189084
12.

Amerindian pyruvate carboxylase deficiency is associated with two distinct missense mutations.

Carbone MA, MacKay N, Ling M, Cole DE, Douglas C, Rigat B, Feigenbaum A, Clarke JT, Haworth JC, Greenberg CR, Seargeant L, Robinson BH.

Am J Hum Genet. 1998 Jun;62(6):1312-9.

13.

Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation.

Laitinen A, Hietala M, Haworth JC, Schroeder ML, Seargeant LE, Greenberg CR, Aula P.

Clin Genet. 1997 Mar;51(3):174-8.

PMID:
9137882
14.

Rickets still affects Canadian children.

Haworth JC.

CMAJ. 1995 Sep 15;153(6):740-1. No abstract available.

15.

A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type I.

Greenberg CR, Reimer D, Singal R, Triggs-Raine B, Chudley AE, Dilling LA, Philipps S, Haworth JC, Seargeant LE, Goodman SI.

Hum Mol Genet. 1995 Mar;4(3):493-5. No abstract available.

PMID:
7795610
16.

Blood lactate and pyruvate concentrations, and their ratio during exercise in healthy children: developmental perspective.

Pianosi P, Seargeant L, Haworth JC.

Eur J Appl Physiol Occup Physiol. 1995;71(6):518-22.

PMID:
8983919
17.

TaqI polymorphism in intron 2 of the GCDH gene.

Haworth JC, Singal R, Goodman SI, Greenberg CR.

Hum Mol Genet. 1994 Apr;3(4):678. No abstract available.

PMID:
8069322
18.

Glycogen storage disease in adults.

Talente GM, Coleman RA, Alter C, Baker L, Brown BI, Cannon RA, Chen YT, Crigler JF Jr, Ferreira P, Haworth JC, Herman GE, Issenman RM, Keating JP, Linde R, Roe TF, Senior B, Wolfsdorf JI.

Ann Intern Med. 1994 Feb 1;120(3):218-26. Review.

PMID:
8273986
19.

Vitamin D deficiency in a Manitoba community.

Lebrun JB, Moffatt ME, Mundy RJ, Sangster RK, Postl BD, Dooley JP, Dilling LA, Godel JC, Haworth JC.

Can J Public Health. 1993 Nov-Dec;84(6):394-6.

PMID:
8131142
20.

A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites.

Greenberg CR, Taylor CL, Haworth JC, Seargeant LE, Philipps S, Triggs-Raine B, Chodirker BN.

Genomics. 1993 Jul;17(1):215-7.

PMID:
8406453
21.

Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers.

Haworth JC, Dilling LA, Surtees RA, Seargeant LE, Lue-Shing H, Cooper BA, Rosenblatt DS.

Am J Med Genet. 1993 Mar 1;45(5):572-6.

PMID:
8456826
22.

Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family.

Haworth JC, Demaugre F, Booth FA, Dilling LA, Moroz SP, Seshia SS, Seargeant LE, Coates PM.

J Pediatr. 1992 Oct;121(4):553-7.

PMID:
1403388
23.

Carrier detection in glutaric aciduria type I using interleukin-2-dependent cultured lymphocytes.

Seargeant LE, Chudley AE, Dilling LA, Mallory CJ, Haworth JC.

J Inherit Metab Dis. 1992;15(5):733-7.

PMID:
1434513
24.

Aspartylglycosaminuria presenting with hepatosplenomegaly in early infancy.

Haworth JC, Seargeant LE, Dilling LA.

J Inherit Metab Dis. 1992;15(6):933-4. No abstract available.

PMID:
1293392
25.
26.

Primary oxaluria type 2 (L-glyceric aciduria): a rare cause of nephrolithiasis in children.

Seargeant LE, deGroot GW, Dilling LA, Mallory CJ, Haworth JC.

J Pediatr. 1991 Jun;118(6):912-4. No abstract available.

PMID:
2040928
27.

Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds.

Haworth JC, Booth FA, Chudley AE, deGroot GW, Dilling LA, Goodman SI, Greenberg CR, Mallory CJ, McClarty BM, Seshia SS, et al.

J Pediatr. 1991 Jan;118(1):52-8.

PMID:
1986098
28.

Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers.

Greenberg CR, Evans JA, McKendry-Smith S, Redekopp S, Haworth JC, Mulivor R, Chodirker BN.

Am J Hum Genet. 1990 Feb;46(2):286-92.

29.

Myopathy with hypophosphatasia.

Seshia SS, Derbyshire G, Haworth JC, Hoogstraten J.

Arch Dis Child. 1990 Jan;65(1):130-1.

30.

Newborn screening for galactosemia: a new method used in Manitoba.

Greenberg CR, Dilling LA, Thompson R, Ford JD, Seargeant LE, Haworth JC.

Pediatrics. 1989 Aug;84(2):331-5.

PMID:
2748263
31.

Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibship.

Booth FA, Haworth JC, Dilling LA, Perry TL, Greenberg CR, Seargeant LE, Penn AM, Rhead WJ.

J Pediatr. 1989 Jul;115(1):81-8.

PMID:
2738799
32.

Vitamin-D-deficient rickets in Manitoba, 1972-84.

Haworth JC, Dilling LA.

CMAJ. 1986 Feb 1;134(3):237-41.

33.

Brain amino acid abnormalities in pyruvate carboxylase deficiency.

Perry TL, Haworth JC, Robinson BH.

J Inherit Metab Dis. 1985;8(2):63-6.

PMID:
2878111
34.

A new form of insulin resistance with growth retardation, fatty liver, and hypogonadotropic hypogonadism.

Tokuhiro E, Dean H, Winter J, Haworth JC, Imai Y, Friesen HG.

Pediatr Res. 1984 Jul;18(7):670-4.

PMID:
6382136
35.

Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.

Schuh S, Rosenblatt DS, Cooper BA, Schroeder ML, Bishop AJ, Seargeant LE, Haworth JC.

N Engl J Med. 1984 Mar 15;310(11):686-90.

PMID:
6700644
36.

The pharmacokinetics of theophylline in an infant with hepatic failure.

Simons FE, Simons KJ, Luciuk GH, Haworth JC.

Dev Pharmacol Ther. 1982;4(3-4):132-8.

PMID:
7172970
37.

Growth and nutrition of preschool Indian children in Manitoba: II. Nutrient intakes.

Ellestad-Sayed JJ, Haworth JC, Coodin FJ, Dilling LA.

Can J Public Health. 1981 Mar-Apr;72(2):127-33. No abstract available.

PMID:
7237347
38.

Lactic acidosis due to pyruvate carboxylase deficiency.

Haworth JC, Robinson BH, Perry TL.

J Inherit Metab Dis. 1981;4(2):57-8.

PMID:
6790846
39.

The Children's Hospital of Winnipeg Research Foundation.

Haworth JC, Chernick V.

Can Med Assoc J. 1980 Dec 20;123(12):1233-4. No abstract available.

40.

Relation of maternal cigarette smoking, obesity, and energy consumption to infant size.

Haworth JC, Ellestad-Sayed JJ, King J, Dilling LA.

Am J Obstet Gynecol. 1980 Dec 15;138(8):1185-9.

PMID:
7446628
41.

Growth and nutrition of Manitoba preschool Indian children. III. Anthropometry.

Coodin FJ, Dilling LA, Haworth JC, Ellestad-Sayed J.

Hum Biol. 1980 Sep;52(3):563-78. No abstract available.

PMID:
7450734
42.

Fetal growth retardation in cigarette-smoking mothers is not due to decreased maternal food intake.

Haworth JC, Ellestad-Sayed JJ, King J, Dilling LA.

Am J Obstet Gynecol. 1980 Jul 15;137(6):719-23.

PMID:
7395936
43.

Defect in soluble tyrosine aminotransferase in skin fibroblasts of a patient with tyrosinemia.

deGroot GW, Dakshinamurti K, Allan L, Haworth JC.

Pediatr Res. 1980 Jul;14(7):896-8. No abstract available.

PMID:
6106182
44.

A case of leprechaunism with severe hyperinsulinemia.

Rosenberg AM, Haworth JC, Degroot GW, Trevenen CL, Rechler MM.

Am J Dis Child. 1980 Feb;134(2):170-5.

PMID:
6986080
45.

Breast-feeding protects against infection in Indian infants.

Ellestad-Sayed J, Coodin FJ, Dilling LA, Haworth JC.

Can Med Assoc J. 1979 Feb 3;120(3):295-8.

46.

Disaccharide malabsorption and dietary patterns in two Canadian Eskimo communities.

Ellestad-Sayed JJ, Haworth JC, Hildes JA.

Am J Clin Nutr. 1978 Aug;31(8):1473-8. No abstract available.

PMID:
581038
47.

Growth and nutrition of preschool Indian children in Manitoba: I. Vitamin D deficiency.

Dilling LA, Ellestad-Sayed J, Coodin FJ, Haworth JC.

Can J Public Health. 1978 May-Jun;69(3):248-52. No abstract available.

PMID:
667774
48.

Protein-energy malnutrition.

Coodin FJ, Haworth JC, Sayed JE.

Can Med Assoc J. 1978 Apr 8;118(7):775. No abstract available.

49.

Severe mental retardation, cataracts, short stature, and primary hypogonadism in two brothers.

Martsolf JT, Hunter AG, Haworth JC.

Am J Med Genet. 1978;1(3):291-9.

PMID:
677168
50.

Breast-feeding by mothers positive for HBsAG.

Larke RP, Haworth JC, Read JH.

Can Med Assoc J. 1977 Jun 18;116(12):1344. No abstract available.

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