M.G Zaahl: search on Z-Library

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1

Multiple endocrine neoplasia syndromes, children, Hirschsprung’s disease and RET

S. W. Moore, M. G. Zaahl

Journal:

Pediatric Surgery International

Year:

2008

Language:

english

File:

PDF, 239 KB

english, 2008

2

The −237C→T promoter polymorphism of theSLC11A1gene is associated with a protective effect in relation to inflammatory bowel disease in the South African population

Monique G. Zaahl, Trevor A. Winter, Louise Warnich, Maritha J. Kotze

Journal:

International Journal of Colorectal Disease

Year:

2006

Language:

english

File:

PDF, 115 KB

english, 2006

3

Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload

Monique G. Zaahl, Alison T. Merryweather-Clarke, Maritha J. Kotze, Schalk van der Merwe, Louise Warnich, Kathryn J. H. Robson

Journal:

Year:

2004

Language:

english

File:

PDF, 316 KB

english, 2004

4

Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population

MJ Kotze, JNP De Villiers, CSH Bouwens, L Warnich, MG Zaahl, S Van Der Merwe, C Oberkanins

Journal:

Clinical Genetics

Year:

2004

Language:

english

File:

PDF, 171 KB

english, 2004

5

Molecular analysis of Ceruloplasmin in a South African cohort presenting with oesophageal cancer

Natalie J. Strickland, Tandi Matsha, Rajief T. Erasmus, Monique G. Zaahl

Journal:

International Journal of Cancer

Year:

2012

Language:

english

File:

PDF, 253 KB

english, 2012

6

Association of functional polymorphisms of SLC11A1 with risk of esophageal cancer in the South African Colored population

Monique G. Zaahl, Louise Warnich, Tommy C. Victor, Maritha J. Kotze

Journal:

Cancer Genetics and Cytogenetics

Year:

2005

Language:

english

File:

PDF, 175 KB

english, 2005

7

Expression of the SLC11A1 (NRAMP1) 5′-(GT)n repeat: Opposite effect in the presence of −237C→T

Monique G Zaahl, Kathryn J.H Robson, Louise Warnich, Maritha J Kotze

Journal:

Blood Cells, Molecules, and Diseases

Year:

2004

Language:

english

File:

PDF, 386 KB

english, 2004

8

Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2

Samuel W. Moore, Justus Appfelstaedt, Monique G. Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2007

Language:

english

File:

PDF, 118 KB

english, 2007

9

Association of endothelin-β receptor (EDNRB) gene variants in anorectal malformations

Sam W. Moore, Monique G. Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2007

Language:

english

File:

PDF, 103 KB

english, 2007

10

A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling

Samuel W. Moore, Monique G. Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2008

Language:

english

File:

PDF, 147 KB

english, 2008

11

The ITGB2 immunomodulatory gene (CD18), enterocolitis, and Hirschsprung's disease

Sam W. Moore, Daniel Sidler, Monique G. Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2008

Language:

english

File:

PDF, 178 KB

english, 2008

12

Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease

Samuel W. Moore, Monique Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2009

Language:

english

File:

PDF, 171 KB

english, 2009

13

Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 “Janus” genetic variation

Sam W. Moore, Monique Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2010

Language:

english

File:

PDF, 256 KB

english, 2010

14

Intronic RET gene variants in Down syndrome–associated Hirschsprung disease in an African population

Samuel W. Moore, Monique G. Zaahl

Journal:

Journal of Pediatric Surgery

Year:

2012

Language:

english

File:

PDF, 103 KB

english, 2012

15

Analysis of the three common mutations in the CARD15 gene (R702W, G908R and 1007fs) in South African colored patients with inflammatory bowel disease

M.G. Zaahl, T. Winter, L. Warnich, M.J. Kotze

Journal:

Molecular and Cellular Probes

Year:

2005

Language:

english

File:

PDF, 84 KB

english, 2005

16

Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element

C.F Hoogendijk, C.L Scholtz, S.M Pimstone, E Ehrenborg, J.J P Kastelein, J.C Defesche, R Thiart, L du Plessis, J.N.P de Villiers, M.G Zaahl, R Delport, D.C Rubinsztein, L.J Raffel, C.E Grim, S Mediene

Journal:

Molecular and Cellular Probes

Year:

2003

Language:

english

File:

PDF, 113 KB

english, 2003

17

Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndrome

M.G Zaahl, L du Plessis, L Warnich, M.J Kotze, S.W Moore

Journal:

Molecular and Cellular Probes

Year:

2003

Language:

english

File:

PDF, 102 KB

english, 2003

18

RET promoter variations in familial African degenerative leiomyopathy (ADL): first report of a possible genetic-environmental interaction

C. Van Rensburg, S. W. Moore, M. Zaahl

Journal:

Pediatric Surgery International

Year:

2012

Language:

english

File:

PDF, 164 KB

english, 2012

19

Tissue specific somatic mutations and aganglionosis in Hirschsprung's disease

Moore, Sam W., Zaahl, Monique G.

Journal:

Journal of Pediatric Surgery

Year:

2014

Language:

english

File:

PDF, 209 KB

english, 2014

20

Analysis of the SLC11A1 gene in South African patients with inflammatory bowel disease

Zaahl, Monique G., Winter, Trevor, Peeters, Armand, Marks, Tessa, Warnich, Louise, Robson, Kathryn, Kotze, Maritha

Journal:

Gastroenterology

Year:

2003

Language:

english

File:

PDF, 175 KB

english, 2003

21

Clinical and genetic correlations of familial Hirschsprung’s disease

Moore, Sam W., Zaahl, Monique

Journal:

Journal of Pediatric Surgery

Year:

2015

Language:

english

File:

PDF, 203 KB

english, 2015

22

Iron homeostasis in porphyria cutanea tarda: mutation analysis of promoter regions of CP, CYBRD1, HAMP and SLC40A1

Panton, N. A., Strickland, N. J., Hift, R. J., Warnich, L., Zaahl, M. G.

Journal:

Journal of Clinical Pathology

Year:

2013

Language:

english

File:

PDF, 64 KB

english, 2013

23

Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS)

Moore, Sam W., Fieggen, Karen, Honey, Engela, Zaahl, Monique

Journal:

Journal of Pediatric Surgery

Year:

2015

Language:

english

File:

PDF, 790 KB

english, 2015

24

Biotechnology Innovators To Convene in Cape Town, South Africa: Pharmacogenetics and Precision Medicine Conference (April 7–9, 2016)

Dandara, Collet, Mpye, Keleabetswe, Agenbag, Gloudi, Skelton, Michelle, Zaahl, Monique, Masimirembwa, Collen, Mulder, Nicola, Warnich, Louise, Pepper, Michael

Journal:

Omics A Journal of Integrative Biology

Year:

2015

Language:

english

File:

PDF, 131 KB

english, 2015

25

The Hirschsprung's–multiple endocrine neoplasia connection

Moore, SW, Zaahl, M

Journal:

Year:

2012

Language:

english

File:

PDF, 157 KB

english, 2012

26

Fat Mass and Obesity-Associated (FTO) Gene Polymorphisms Are Associated with Physical Activity, Food Intake, Eating Behaviors, Psychological Health, and Modeled Change in Body Mass Index in Overweight/Obese Caucasian Adults

Harbron, Janetta, van der Merwe, Lize, Zaahl, Monique, Kotze, Maritha, Senekal, Marjanne

Journal:

Year:

2014

Language:

english

File:

PDF, 255 KB

english, 2014

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