Profil bibliographique

N.G.G.M. Abeling

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23Publications signalées

1007Citations signalées

0Affiliations récentes

Domaines associés

Metabolism and Genetic DisordersBiochemical and Molecular ResearchNeonatal Health and BiochemistryGenetics and Neurodevelopmental DisordersNeuroblastoma Research and Treatments

Publications récentes

Accès ouvert 2016 articleOpenAlex

Catecholamines Profiles at Diagnosis: Increased Diagnostic Sensitivity and Correlation with Biological and Clinical Features in Neuroblastoma Patients

I.R.N. Verly, André B. P. Kuilenburg, N.G.G.M. Abeling, Susan Goorden et autres

0 citationsData Archiving and Networked Services (DANS)

2011 articleOpenAlex

Folinic Acid Supplementation in Rett Syndrome Patients Does Not Influence the Course of the Disease: A Randomized Study

Eveline Hagebeuk, Marinus Durán, J.H.T.M. Koelman, N.G.G.M. Abeling et autres

15 citationsJournal of Child Neurology

2009 articleOpenAlex

Numerical Changes in the Various Peripheral White Blood Cells in Children as a Result of Antineoplastic Therapy

E. Cranendonk, A. H. van Gennip, N.G.G.M. Abeling, H. Behrendt

13 citationsActa Haematologica

2009 articleOpenAlex

Evaluation of the Use of the Hemalog D in Acute Lymphoblastic Leukaemia and Disseminated Non-Hodgkin’s Lymphoma in Children

E. Cranendonk, N.G.G.M. Abeling, Arjen Q. Bakker, Michiel E. de Jong et autres

3 citationsActa Haematologica

Accès ouvert 2009 book-reviewOpenAlex

Book Reviews

F. Herrmann, G. Sieber, B. Komischke, R. Oestreich et autres

1 citationActa Haematologica

2009 book-reviewOpenAlex

Book Reviews

M. Konwinski, Jessica Caro, Olcay Batuman, A. J. Erslev et autres

0 citationsActa Haematologica

2006 articleOpenAlex

Quantification of free and total sialic acid excretion by LC–MS/MS

Maria van der Ham, Berthil H.C.M.T. Prinsen, J. G. M. Huijmans, N.G.G.M. Abeling et autres

65 citationsJournal of Chromatography B

2006 articleOpenAlex

A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria

Hennie Bikker, H. D. Bakker, N.G.G.M. Abeling, Bwee Tien Poll‐The et autres

36 citationsHuman Mutation

2006 articleOpenAlex

Sepiapterin reductase deficiency an autosomal recessive DOPA-responsive dystonia

N.G.G.M. Abeling, M. Durán, Hester I. Bakker, Lida E. M. Stroomer et autres

62 citationsMolecular Genetics and Metabolism

Accès ouvert 2004 articleOpenAlex

Quantification of Free Sialic Acid in Urine by HPLC–Electrospray Tandem Mass Spectrometry: A Tool for the Diagnosis of Sialic Acid Storage Disease

Fredoen Valianpour, N.G.G.M. Abeling, Marinus Durán, J. G. M. Huijmans et autres

52 citationsClinical Chemistry

2001 articleOpenAlex

Mild learning difficulties and offending behaviour – is there a link with monoamine oxidase A deficiency?

V. R. Stamps, N.G.G.M. Abeling, A. H. van Gennip, Arno G. van Cruchten et autres

3 citationsPsychiatric Genetics

1998 articleOpenAlex

Aromatic L‐amino acid decarboxylase deficiency: A new case with a mild clinical presentation and unexpected laboratory findings

N.G.G.M. Abeling, A. H. van Gennip, P. G. Barth, Arno van Cruchten et autres

40 citationsJournal of Inherited Metabolic Disease

Notice OpenAlex

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