Viljoen D[au] - Search Results

Year	Number of Results
1971	3
1972	1
1973	1
1974	1
1979	1
1983	4
1984	3
1985	1
1987	12
1988	8
1989	4
1990	3
1991	11
1992	4
1993	5
1994	5
1995	6
1996	2
1997	3
1998	1
1999	4
2000	3
2001	5
2002	4
2003	4
2004	3
2005	6
2006	5
2007	2
2008	3
2009	2
2010	3
2011	4
2012	1
2013	1
2014	1
2015	2
2016	3
2017	3
2018	1
2021	1
2022	1

1

Functional relevance of human adh polymorphism.

Eriksson CJ, Fukunaga T, Sarkola T, Chen WJ, Chen CC, Ju JM, Cheng AT, Yamamoto H, Kohlenberg-Müller K, Kimura M, Murayama M, Matsushita S, Kashima H, Higuchi S, Carr L, Viljoen D, Brooke L, Stewart T, Foroud T, Su J, Li TK, Whitfield JB. Eriksson CJ, et al. Among authors: viljoen d. Alcohol Clin Exp Res. 2001 May;25(5 Suppl ISBRA):157S-163S. doi: 10.1097/00000374-200105051-00027. Alcohol Clin Exp Res. 2001. PMID: 11391066 Review.

2

Tributes.

Sellars SL, Hamersma H, Kozlowski K, Winship I, Medefindt C, Zieff S, Bonafede P, Gericke G, Viljoen DL. Sellars SL, et al. Among authors: viljoen dl. S Afr Med J. 2016 May 25;106(6 Suppl 1):S59-64. doi: 10.7196/SAMJ.2016.v106i6.10996. S Afr Med J. 2016. PMID: 27245529 No abstract available.

3

Congenital contractural arachnodactyly (Beals syndrome).

Viljoen D. Viljoen D. J Med Genet. 1994 Aug;31(8):640-3. doi: 10.1136/jmg.31.8.640. J Med Genet. 1994. PMID: 7815423 Free PMC article. Review.

4

Hearing impairment and pigmentary disturbance.

Beighton P, Ramesar R, Winship I, Viljoen D, Greenberg J, Young K, Curtis D, Sellars S. Beighton P, et al. Among authors: viljoen d. Ann N Y Acad Sci. 1991;630:152-66. doi: 10.1111/j.1749-6632.1991.tb19584.x. Ann N Y Acad Sci. 1991. PMID: 1952586 Review.

5

Mseleni and Handigodu familial osteoarthropathies: syndromic identity?

Agarwal SS, Phadke SR, Fredlund V, Viljoen D, Beighton P. Agarwal SS, et al. Among authors: viljoen d. Am J Med Genet. 1997 Nov 12;72(4):435-9. doi: 10.1002/(sici)1096-8628(19971112)72:4<435::aid-ajmg12>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9375727 Review.

6

The Tensile Behaviour of Highly Filled High-Density Polyethylene Quaternary Composites: Weld-Line Effects, DIC Curiosities and Shifted Deformation Mechanisms.

Viljoen D, Fischer M, Kühnert I, Labuschagné J. Viljoen D, et al. Polymers (Basel). 2021 Feb 10;13(4):527. doi: 10.3390/polym13040527. Polymers (Basel). 2021. PMID: 33579039 Free PMC article.

7

Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation.

Biesecker LG, Happle R, Mulliken JB, Weksberg R, Graham JM Jr, Viljoen DL, Cohen MM Jr. Biesecker LG, et al. Among authors: viljoen dl. Am J Med Genet. 1999 Jun 11;84(5):389-95. doi: 10.1002/(sici)1096-8628(19990611)84:5<389::aid-ajmg1>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10360391 Review.

8

Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome.

Viljoen DL, Jaquire Z, Woods DL. Viljoen DL, et al. Prenat Diagn. 1991 Mar;11(3):167-75. doi: 10.1002/pd.1970110306. Prenat Diagn. 1991. PMID: 2038600 Review.

9

Pseudoxanthoma elasticum (Grönblad-Strandberg syndrome).

Viljoen D. Viljoen D. J Med Genet. 1988 Jul;25(7):488-90. doi: 10.1136/jmg.25.7.488. J Med Genet. 1988. PMID: 3172143 Free PMC article. No abstract available.

10

Klippel-Trenaunay-Weber syndrome (angio-osteohypertrophy syndrome).

Viljoen DL. Viljoen DL. J Med Genet. 1988 Apr;25(4):250-2. doi: 10.1136/jmg.25.4.250. J Med Genet. 1988. PMID: 2835482 Free PMC article. No abstract available.

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