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Search Results - van Maarle, MC
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Association of TNF-α serum levels and TNFA promoter polymorphisms with risk of myocardial infarction
by
Bennet, A.M.
,
van Maarle, M.C.
,
Hallqvist, J.
,
Morgenstern, R.
,
Frostegård, J.
,
Wiman, B.
,
Prince, J.A.
,
de Faire, U.
Published in
Atherosclerosis
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Distal muscle weakness and optic atrophy without central nervous system involvement in a patient with a homozygous missense mutation in the C19ORF12-gene
by
de Vries, R.J.
,
Jaeger, B.
,
Hellebrekers, D.M.E.I.
,
Reneman, L.
,
Verhamme, C.
,
Smeets, H.J.M.
,
van Maarle, M.C.
,
de Visser, M.
,
Bleeker, F.E.
Published in
Clinical neurology and neurosurgery
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Getting insurance after genetic screening on familial hypercholesterolaemia; the need to educate both insurers and the public to increase adherence to national guidelines in the Ne...
by
Marang-van de Mheen, P J
,
van Maarle, M C
,
Stouthard, M E A
Published in
Journal of epidemiology and community health (1979)
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Risk perception of participants in a family-based genetic screening program on familial hypercholesterolemia
by
van Maarle, M.C.
,
Stouthard, M.E.A.
,
Bonsel, G.J.
Published in
American journal of medical genetics. Part A
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How Disturbing Is It to Be Approached for a Genetic Cascade Screening Programme for Familial Hypercholesterolaemia?: Psychological Impact and Screenees’ Views
by
van Maarle, M.C.
,
Stouthard, M.E.A.
,
Marang-v.d., P.J.
,
Klazinga, Mheen N.S.
,
Bonsel, G.J.
Published in
Community genetics
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Follow up after a family based genetic screening programme for familial hypercholesterolaemia: is screening alone enough?
by
van Maarle, Merel C
,
Stouthard, Marlies E A
,
Marang-van de Mheen, Perla J
,
Klazinga, Niek S
,
Bonsel, Gouke J
Published in
BMJ
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How Disturbing Is It to Be Approached for a Genetic Cascade Screening Programme for Familial Hypercholesterolaemia?
by
van Maarle, MC
,
Stouthard, MEA
,
Marang-v.d. Mheen, PJ
,
Klazinga, N S
,
Bonsel, G J
Published in
Community genetics
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