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Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype

Platelets (Edinburgh), 2018-01, Vol.29 (1), p.91-94

2018

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BRAF mutation analysis in fine needle aspiration (FNA) cytology of the thyroid

Diagnostic molecular pathology, 2006-09, Vol.15 (3), p.136-143

2006

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Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience

Seminars in thrombosis and hemostasis, 2018-04, Vol.44 (3), p.287-292

2018

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Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden: A Comparison of Institutional and National Provider Practices

American journal of clinical pathology, 2017-06, Vol.147 (6), p.604-610

2017

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Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant

American journal of medical genetics. Part A, 2018-12, Vol.176 (12), p.2819-2823

2018

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Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden

American journal of clinical pathology, 2017-06, Vol.147 (6), p.604-610

2017

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Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia

Leukemia & lymphoma, 2017-08, Vol.58 (8), p.1963-1967

2017

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Practice patterns in the diagnosis of inherited platelet disorders within a single institution

Blood coagulation & fibrinolysis, 2017-06, Vol.28 (4), p.303-308

2017

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Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family

Platelets (Edinburgh), 2016-10, Vol.27 (7), p.712-715

2016

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Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype

Platelets, 2018, Vol.29 (1), p.91-94

2018

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Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia

Leukemia & lymphoma, 2017, Vol.58 (8), p.1963-1967

2017

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Genetic Study of Patients with Severe Dense Granule Deficiency: Unraveling the Underlying Genetic Complexity of Hermansky-Pudlak Syndrome

Blood, 2023-11, Vol.142 (Supplement 1), p.1221-1221

2023

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How Flexible is the Use of Egocentric Versus Allocentric Frame of Reference in the Williams Syndrome Population?

Archives of clinical neuropsychology, 2018-08, Vol.33 (5), p.619-630

2018

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SARS-CoV-2 epitope-specific CD4 + memory T cell responses across COVID-19 disease severity and antibody durability

Science immunology, 2022-07, Vol.7 (73), p.eabl9464

2022

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Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency

Blood coagulation & fibrinolysis, 2021-07, Vol.32 (5), p.344-348

2021

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Low-dose methadone added to another opioid for cancer pain: a multicentre prospective study

Supportive care in cancer, 2024-11, Vol.32 (11), p.716, Article 716

2024

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Surgical management of acute cholecystitis: results of a 2-year prospective multicenter survey in Belgium

Surgical endoscopy, 2012-09, Vol.26 (9), p.2436-2445

2012

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Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients

British journal of haematology, 2020-09, Vol.190 (5), p.e316-e320

2020

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The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease Defects in Cystic Fibrosis Cells

Cells (Basel, Switzerland), 2024-01, Vol.13 (2)

2024

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The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease (MBTP1) Alleviates the p.Phe508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Defects in Cystic Fibrosis Cells

Cells (Basel, Switzerland), 2024-01, Vol.13 (2), p.185

2024

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L'invention » de l'immigré. La psychiatrie belge face à la migration maghrébine dans les années 1960 et 1970

Mouvement social, 2013-02, Vol.242 (1), p.31-44

2013

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The invention of the immigrant. Belgian psychiatry faced with North African immigration in the 1960s-70s

Mouvement social, 2013-01, Vol.242, p.31-44

2013

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L'invention » de l'immigré. La psychiatrie belge face à la migration maghrébine dans les années 1960 et 1970

Mouvement social, 2013-01 (242), p.31-44

2013

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L’invention » de l’immigré. La psychiatrie belge face à la migration maghrébine dans les années 1960 et 1970

Mouvement social, 2013, Vol.242 (1), p.31-44

2013

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Impaired semantic knowledge underlies the reduced verbal short-term storage capacity in Alzheimer's disease

Neuropsychologia, 2009-12, Vol.47 (14), p.3067-3073

2009

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Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype

BRAF mutation analysis in fine needle aspiration (FNA) cytology of the thyroid

Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience

Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden: A Comparison of Institutional and National Provider Practices

Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant

Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden

Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia

Practice patterns in the diagnosis of inherited platelet disorders within a single institution

Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family

Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype

Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia

Genetic Study of Patients with Severe Dense Granule Deficiency: Unraveling the Underlying Genetic Complexity of Hermansky-Pudlak Syndrome

How Flexible is the Use of Egocentric Versus Allocentric Frame of Reference in the Williams Syndrome Population?

SARS-CoV-2 epitope-specific CD4 + memory T cell responses across COVID-19 disease severity and antibody durability

Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency

Low-dose methadone added to another opioid for cancer pain: a multicentre prospective study

Surgical management of acute cholecystitis: results of a 2-year prospective multicenter survey in Belgium

Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients

The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease Defects in Cystic Fibrosis Cells

The Inhibition of the Membrane-Bound Transcription Factor Site-1 Protease (MBTP1) Alleviates the p.Phe508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Defects in Cystic Fibrosis Cells

L'invention » de l'immigré. La psychiatrie belge face à la migration maghrébine dans les années 1960 et 1970

The invention of the immigrant. Belgian psychiatry faced with North African immigration in the 1960s-70s

L'invention » de l'immigré. La psychiatrie belge face à la migration maghrébine dans les années 1960 et 1970

L’invention » de l’immigré. La psychiatrie belge face à la migration maghrébine dans les années 1960 et 1970

Impaired semantic knowledge underlies the reduced verbal short-term storage capacity in Alzheimer's disease

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