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response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study

Journal of inherited metabolic disease, 2007-10, Vol.30 (5), p.700-707

2007

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Hyperargininemia due to liver arginase deficiency

Molecular genetics and metabolism, 2005-03, Vol.84 (3), p.243-251

2005

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T719 PERCUTANEOUS PULSED RADIOFREQUENCY TREATMENT OF ATYPICAL FACIAL PAIN: A STUDY OF 3 CASES

European journal of pain supplements, 2011-09, Vol.5 (1), p.100-100

2011

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Seven‐year safety and efficacy with velaglucerase alfa for treatment‐naïve adult patients with type 1 Gaucher disease

American journal of hematology, 2015-07, Vol.90 (7), p.577-583

2015

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Nutritional management in adults with glycogen storage disease type Ia (GSDIa) enrolled in a phase 1/2 clinical trial of an AAV8-mediated liver-directed gene therapy

Molecular genetics and metabolism, 2022-05, Vol.136, p.S19

2022

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P.24 - Nutritional management in adults with glycogen storage disease type Ia (GSDIa) enrolled in a phase 1/2 clinical trial of an AAV8-mediated liver-directed gene therapy

Molecular genetics and metabolism, 2022-05, Vol.136, p.S19-S19

2022

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Central pain: an overview

Acta neurologica Belgica, 2002-09, Vol.102 (3), p.97-103

2002

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Tolérance et efficacité d’un traitement à long terme par vélaglucérase alfa chez des adultes atteints de la maladie de gaucher de type 1 et naïfs de traitement : résultats issus des études de phase III

La revue de medecine interne, 2015-06, Vol.36, p.A106-A107

2015

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Ketamine: een snelwerkende behandelingsstrategie bij depressie?

Tijdschrift voor geneeskunde, 2015 (17), p.1095-1103

2015

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Efficacité et tolérance à long terme d’une enzymothérapie substitutive la vélaglucérase alfa, chez les patients atteints de la maladie de gaucher de type 1 qui ont switché de l’imiglucérase

La revue de medecine interne, 2015-06, Vol.36, p.A108-A108

2015

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Traitement à long terme par une enzymothérapie substitutive la vélaglucérase alfa chez des enfants atteints de la maladie de gaucher de type 1

La revue de medecine interne, 2015-06, Vol.36, p.A107-A108

2015

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Haemodynamic and electroencephalographic response to insertion of a cuffed oropharyngeal airway: comparison with the laryngeal mask airway

British journal of anaesthesia : BJA, 1998-09, Vol.81 (3), p.393-397

1998

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1261 Enzyme Replacement Therapy with Velaglucerase Alfa Improves Key Clinical Parameters in a Pediatric Subgroup with Type 1 Gaucher Disease

Pediatric research, 2010-11, Vol.68 (Suppl 1), p.625-625

2010

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Pharmacokinetics of Sapropterin in Patients with Phenylketonuria

Clinical pharmacokinetics, 2008-01, Vol.47 (12), p.817-825

2008

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Two-Year Safety and Tolerability of Velaglucerase Alfa in Patients with Type 1 Gaucher Disease, Including Patients Switched From Imiglucerase: Phase III Trial HGT-GCB-039 and Extension

Blood, 2011-11, Vol.118 (21), p.3214-3214

2011

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482 Safety and Efficacy of Velaglucerase Alfa in Gaucher Disease Type 1 Patients Previously Treated with Imiglucerase

Pediatric research, 2010-11, Vol.68 (Suppl 1), p.246-247

2010

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Pitfalls in Newborn Screening

The Journal of pediatrics, 2005-07, Vol.147 (1), p.119-120

2005

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Efficacy of spinal cord stimulation for neuropathic pain: assessment by abstinenceMonhemius R, Simpson B, Eur J Pain 2003,7;513–9

European journal of pain, 2005-02, Vol.9 (1), p.95

2005

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Comment on ‘Pulsed radiofrequency treatment of the gasserian ganglion in patients with idiopathic trigeminal neuralgia’

Pain (Amsterdam), 2004, Vol.107 (1), p.195-195

2004

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Efficacy of spinal cord stimulation for neuropathic pain: assessment by abstinence: Monhemius R, Simpson B, Eur J Pain 2003,7;513–9

European journal of pain, 2005-02, Vol.9 (1), p.95-95

2005

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Construction of human embryonic cDNA libraries: HD, PKD1 and BRCA1 are transcribed widely during embryogenesis

Cytogenetic and genome research, 1995-01, Vol.71 (2), p.197-202

1995

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Transcription patterns of sequences on human chromosome 21

Cytogenetic and genome research, 1995-01, Vol.71 (2), p.203-206

1995

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Beschouwingen rond palliatieve terminale sedatie

Tijdschrift voor geneeskunde, 2004-01 (3), p.159-163

2004

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Beschouwingen rond palliatieve terminale sedatie

Tijdschrift voor geneeskunde, 2004-01, Vol.60 (3), p.159-163

2004

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Separation of some cephalosporin derivatives by ion-pair reversed-phase high-performance liquid chromatography

Journal of Chromatography A, 1979-02, Vol.169, p.343-350

1979

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response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study

Hyperargininemia due to liver arginase deficiency

T719 PERCUTANEOUS PULSED RADIOFREQUENCY TREATMENT OF ATYPICAL FACIAL PAIN: A STUDY OF 3 CASES

Seven‐year safety and efficacy with velaglucerase alfa for treatment‐naïve adult patients with type 1 Gaucher disease

Nutritional management in adults with glycogen storage disease type Ia (GSDIa) enrolled in a phase 1/2 clinical trial of an AAV8-mediated liver-directed gene therapy

P.24 - Nutritional management in adults with glycogen storage disease type Ia (GSDIa) enrolled in a phase 1/2 clinical trial of an AAV8-mediated liver-directed gene therapy

Central pain: an overview

Tolérance et efficacité d’un traitement à long terme par vélaglucérase alfa chez des adultes atteints de la maladie de gaucher de type 1 et naïfs de traitement : résultats issus des études de phase III

Ketamine: een snelwerkende behandelingsstrategie bij depressie?

Efficacité et tolérance à long terme d’une enzymothérapie substitutive la vélaglucérase alfa, chez les patients atteints de la maladie de gaucher de type 1 qui ont switché de l’imiglucérase

Traitement à long terme par une enzymothérapie substitutive la vélaglucérase alfa chez des enfants atteints de la maladie de gaucher de type 1

Haemodynamic and electroencephalographic response to insertion of a cuffed oropharyngeal airway: comparison with the laryngeal mask airway

1261 Enzyme Replacement Therapy with Velaglucerase Alfa Improves Key Clinical Parameters in a Pediatric Subgroup with Type 1 Gaucher Disease

Pharmacokinetics of Sapropterin in Patients with Phenylketonuria

Two-Year Safety and Tolerability of Velaglucerase Alfa in Patients with Type 1 Gaucher Disease, Including Patients Switched From Imiglucerase: Phase III Trial HGT-GCB-039 and Extension

482 Safety and Efficacy of Velaglucerase Alfa in Gaucher Disease Type 1 Patients Previously Treated with Imiglucerase

Pitfalls in Newborn Screening

Efficacy of spinal cord stimulation for neuropathic pain: assessment by abstinenceMonhemius R, Simpson B, Eur J Pain 2003,7;513–9

Comment on ‘Pulsed radiofrequency treatment of the gasserian ganglion in patients with idiopathic trigeminal neuralgia’

Efficacy of spinal cord stimulation for neuropathic pain: assessment by abstinence: Monhemius R, Simpson B, Eur J Pain 2003,7;513–9

Construction of human embryonic cDNA libraries: HD, PKD1 and BRCA1 are transcribed widely during embryogenesis

Transcription patterns of sequences on human chromosome 21

Beschouwingen rond palliatieve terminale sedatie

Beschouwingen rond palliatieve terminale sedatie

Separation of some cephalosporin derivatives by ion-pair reversed-phase high-performance liquid chromatography

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