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Development, validation and evaluation of a rapid PCR-nucleic acid lateral flow immuno-assay for the detection of Plasmodium and the differentiation between Plasmodium falciparum and Plasmodium vivax

Malaria journal, 2012-08, Vol.11 (1), p.279-279, Article 279

2012

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Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

Brain (London, England : 1878), 2011-01, Vol.134 (Pt 1), p.143-156

2011

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Systemic complement activation in deceased donors is associated with acute rejection after renal transplantation in the recipient

Transplantation, 2011-07, Vol.92 (2), p.163-169

2011

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The influence of deceased donor age and old-for-old allocation on kidney transplant outcome

Transplantation, 2009-08, Vol.88 (4), p.542-552

2009

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Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation

The Journal of clinical investigation, 2002-09, Vol.110 (6), p.807-814

2002

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CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two children

Neuropediatrics, 2004-02, Vol.35 (1), p.45-49

2004

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Interpretation of Restriction Fragment Length Polymorphism Analysis of Mycobacterium tuberculosis Isolates from a State with a Large Rural Population

The Journal of infectious diseases, 1997-06, Vol.175 (6), p.1446-1452

1997

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Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

Human genetics, 2004, Vol.114 (2), p.149-156

2004

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MR Imaging Features in Marinesco-Sjogren Syndrome: Severe Cerebellar Atrophy Is Not an Obligatory Finding

American journal of neuroradiology : AJNR, 2003-05, Vol.24 (5), p.825-828

2003

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Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Neuropediatrics, 2003-08, Vol.34 (4), p.215-218

2003

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Large cerebral vessel occlusive disease in Lyme neuroborreliosis

Neuropediatrics, 2002-02, Vol.33 (1), p.37-40

2002

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Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

Neuromuscular disorders : NMD, 2000-12, Vol.10 (8), p.572-577

2000

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Comparison of three immunoassays for diagnosing sensitization to latex in children with spina bifida

Pediatric allergy and immunology, 1996-11, Vol.7 (4), p.164-166

1996

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Short-course chemotherapy for tuberculosis in children

Pediatrics (Evanston), 1983-12, Vol.72 (6), p.801-806

1983

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MEN-2 syndrome: the value of screening and central registration; a study of six kindreds in The Netherlands

Henry Ford Hospital medical journal, 1987, Vol.35 (2-3), p.101

1987

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Development, validation and evaluation of a rapid PCR-nucleic acid lateral flow immuno-assay for the detection of Plasmodium and the differentiation between Plasmodium falciparum and Plasmodium vivax

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

Systemic complement activation in deceased donors is associated with acute rejection after renal transplantation in the recipient

The influence of deceased donor age and old-for-old allocation on kidney transplant outcome

Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation

CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two children

Interpretation of Restriction Fragment Length Polymorphism Analysis of Mycobacterium tuberculosis Isolates from a State with a Large Rural Population

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

MR Imaging Features in Marinesco-Sjogren Syndrome: Severe Cerebellar Atrophy Is Not an Obligatory Finding

Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Large cerebral vessel occlusive disease in Lyme neuroborreliosis

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

Comparison of three immunoassays for diagnosing sensitization to latex in children with spina bifida

Short-course chemotherapy for tuberculosis in children

MEN-2 syndrome: the value of screening and central registration; a study of six kindreds in The Netherlands

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