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1 . Periodical
The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine
저자
by
Broekman, M M T J
;
Wong, D R
;
Wanten, G J A
;
Roelofs, H M
;
van Marrewijk, C J
, et al.
소스
The Pharmacogenomics Journal; January 2018, Vol. 18 Issue: 1 p160-166, 7p
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7 . Academic Journal
Autosomal recessive cerebellar ataxias: the current state of affairs
저자
by
Vermeer, S
;
van de Warrenburg, B P C
;
Willemsen, M A A P
;
Cluitmans, M
;
Scheffer, H
, et al.
소스
Journal of Medical Genetics
. Oct 01, 2011 48(10):651-659
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7 . Academic Journal
Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations
저자
by
de Bot, S T
;
van den Elzen, R T M
;
Mensenkamp, A R
;
Schelhaas, H J
;
Willemsen, M A A P
, et al.
소스
Journal of Neurology, Neurosurgery & Psychiatry
. Oct 01, 2010 81(10):1073-1078
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7 . Academic Journal
A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum
저자
by
van Reeuwijk, J
;
Olderode-Berends, M JW
;
van den Elzen, C
;
Brouwer, O F
;
Roscioli, T
, et al.
소스
Clinical Genetics
. Sep 01, 2010 78(3):275-281
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7 . Academic Journal
Mevalonate kinase deficiency: Evidence for a phenotypic continuum.
저자
by
Simon A
;
Kremer HPH
;
Wevers RA
;
Scheffer H
;
de Jong JG
, et al.
소스
Neurology; 2004 Mar 23, Vol. 62 Issue 6, p994-997, 4p
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7 . Academic Journal
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
저자
by
van de Warrenburg, B P C
;
Sinke, R J
;
Verschuuren-Bemelmans, C C
;
Scheffer, H
;
Brunt, E R
, et al.
소스
Neurology; 2002 Mar 12, Vol. 58 Issue 5, p702-708, 7p
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7 . Academic Journal
Gene expression profiling in rheumatoid arthritis: current concepts and future directions
저자
by
Toonen, E J M
;
Barrera, P
;
Radstake, T R D J
;
van Riel, P L C M
;
Scheffer, H
, et al.
소스
Annals of the Rheumatic Diseases
. Dec 01, 2008 67(12):1663-1669
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7 . Academic Journal
The tumour necrosis factor receptor superfamily member 1b 676T>G polymorphism in relation to response to infliximab and adalimumab treatment and disease severity in rheumatoid arthritis
저자
by
Toonen, E J M
;
Coenen, M J H
;
Kievit, W
;
Fransen, J
;
Eijsbouts, A M
, et al.
소스
Annals of the Rheumatic Diseases
. Aug 01, 2008 67(8):1174-1177
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7 . Academic Journal
Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chart.
저자
by
Rake, Jan Peter
;
ten Berge, Annelies M.
;
Visser, Gepke
;
Verlind, Edwin
;
Niezen-Koning, Klary E.
, et al.
소스
European Journal of Pediatrics
. 2000, Vol. 159 Issue 5, p322-330. 9p.
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7 . Academic Journal
The association between HTR2C polymorphisms and obesity in psychiatric patients using antipsychotics: a cross-sectional study
저자
by
Mulder, H
;
Franke, B
;
Aart van der - Beek van der, A
;
Arends, J
;
Wilmink, F W
, et al.
소스
The Pharmacogenomics Journal
. Oct 01, 2007 7(5):318-324
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