Vallance H - Search Results

1

Mucopolysaccharidosis type VII (Sly syndrome) presenting as neonatal cholestasis with hepatosplenomegaly.

Gillett PM, Schreiber RA, Jevon GP, Israel DM, Warshawski T, Vallance H, Clarke LA. Gillett PM, et al. Among authors: vallance h. J Pediatr Gastroenterol Nutr. 2001 Aug;33(2):216-20. doi: 10.1097/00005176-200108000-00025. J Pediatr Gastroenterol Nutr. 2001. PMID: 11568529 Review. No abstract available.

2

Pseudo-lysosomal storage disease caused by EMLA cream.

Vallance H, Chaba T, Clarke L, Taylor G. Vallance H, et al. J Inherit Metab Dis. 2004;27(4):507-11. doi: 10.1023/B:BOLI.0000037352.98317.5a. J Inherit Metab Dis. 2004. PMID: 15303008

3

A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathy.

Leary SC, Mattman A, Wai T, Koehn DC, Clarke LA, Chan S, Lomax B, Eydoux P, Vallance HD, Shoubridge EA. Leary SC, et al. Mol Genet Metab. 2006 Sep-Oct;89(1-2):129-33. doi: 10.1016/j.ymgme.2006.04.016. Epub 2006 Jun 9. Mol Genet Metab. 2006. PMID: 16765077

4

A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.

Vallance HD, Jeven G, Wallace DC, Brown MD. Vallance HD, et al. Pediatr Cardiol. 2004 Sep-Oct;25(5):538-40. doi: 10.1007/s00246-003-0446-y. Epub 2004 May 28. Pediatr Cardiol. 2004. PMID: 15164143

5

Serum Betaine and Dimethylglycine Are Higher in South Asian Compared with European Pregnant Women in Canada, with Betaine and Total Homocysteine Inversely Associated in Early and Midpregnancy, Independent of Ethnicity.

Mujica-Coopman MF, Tan A, Schroder TH, Sinclair G, Vallance HD, Lamers Y. Mujica-Coopman MF, et al. Among authors: vallance hd. J Nutr. 2019 Dec 1;149(12):2145-2155. doi: 10.1093/jn/nxz178. J Nutr. 2019. PMID: 31504713 Free article.

6

Rapid, semi-quantitative assay of C-reactive protein evaluated.

Vallance H, Lockitch G. Vallance H, et al. Clin Chem. 1991 Nov;37(11):1981-2. Clin Chem. 1991. PMID: 1934474

7

Novel point mutation (W184R) in neonatal type 2 Gaucher disease.

Choy FY, Wong K, Vallance HD, Baldwin V. Choy FY, et al. Among authors: vallance hd. Pediatr Dev Pathol. 2000 Mar-Apr;3(2):180-3. doi: 10.1007/s100240050023. Pediatr Dev Pathol. 2000. PMID: 10679038

8

Biochemical approach to the investigation of pediatric mitochondrial disease.

Vallance H. Vallance H. Pediatr Dev Pathol. 2004 Nov-Dec;7(6):633-6. doi: 10.1007/s10024-004-5053-2. Epub 2004 Nov 17. Pediatr Dev Pathol. 2004. PMID: 15630534 Review. No abstract available.

9

The Brugada ECG pattern in a neonate.

Sanatani S, Mahkseed N, Vallance H, Brugada R. Sanatani S, et al. Among authors: vallance h. J Cardiovasc Electrophysiol. 2005 Mar;16(3):342-4. doi: 10.1046/j.1540-8167.2005.40607.x. J Cardiovasc Electrophysiol. 2005. PMID: 15817096

10

Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: a unique patient or a novel metabolic disorder?

Waters PJ, Khashu M, Lillquist Y, Senger C, Mattman A, Demos M, Setchell K, Rupar A, Scott P, Blau N, Vallance HD. Waters PJ, et al. Mol Genet Metab. 2005 Dec;86 Suppl 1:S148-52. doi: 10.1016/j.ymgme.2005.07.032. Epub 2005 Sep 21. Mol Genet Metab. 2005. PMID: 16182582

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