Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Malou Ngalula Mujinga"'
Autor:
Laurence Dedeken, Rudy Chapusette, Phu Quoc Lê, Catherine Heijmans, Christine Devalck, Sophie Huybrechts, France Ziereisen, Laurence Hanssens, Laurence Rozen, Denis Noubouossie, Malou Ngalula Mujinga, Alina Ferster
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e108922 (2014)
BACKGROUND:The 6-minute walk test (6 MWT) is used in adults and children affected by a wide range of chronic diseases to evaluate their sub-maximal exercise capacity. It reflects the global response of various physiological systems in a situation sim
Externí odkaz:
https://doaj.org/article/321f11c6f87e4006a20f3af001373f8c
Autor:
Christine Devalck, Michel Ntetani Aloni, Phu Quoc Lê, Nadira Azzi, Sophie Huybrechts, Catherine Heijmans, Alina Ferster, Malou Ngalula-Mujinga
Publikováno v:
Hematology. 20:284-288
Objective Red cell exchange transfusion is frequently used in the management of patients with sickle cell disease (SCD) either electively or chronically to maintain hemoglobin S (HbS)
Autor:
Catherine Heijmans, Alina Ferster, Laurence Rozen, Malou Ngalula Mujinga, Christine Devalck, Laurence Hanssens, Sabine Amah, Geoffrey Bourg, Rossana Pavone, Safiatou Diallo, Phu Quoc Lê, Laurence Dedeken
Publikováno v:
Blood. 132:1085-1085
The six-minute walk test (6MWT) was introduced in adults and children suffering from pulmonary or cardio-vascular conditions to assess their sub-maximal functional exercise capacity. In sickle cell disease (SCD), a reduced 6-minute walk distance was
Autor:
Malou Ngalula-Mujinga, Nadira Azzi, Sophie Huybrechts, Christine Devalck, Catherine Heijmans, Alina Ferster, Pauline Lecerf, Phu Quoc Lê, Michel Ntetani Aloni
Publikováno v:
Hematology (Amsterdam, Netherlands). 20(7)
For centuries, writers have recorded their observations on pica. Nevertheless the association of pica with sickle cell disease (SCD) was poorly documented.Cross-sectional evaluation performed on SCD children and caregivers attending the outpatient cl
Autor:
J Fontaine, F. D. Pooter, Sophie Huybrechts, Phu Quoc Lê, S. Redant, Alina Ferster, J L Wayenberg, Malou Ngalula Mujinga, Laurence Dedeken, Catherine Heijmans
Publikováno v:
Archives of Disease in Childhood. 97:A456-A457
Pain resulting from sickle-cell vaso-occlusive crisis (VOC) is often severe, prolonged and difficult to alleviate. Guidelines based on scientific evidence are lacking. In order to evaluate the effectiveness of our treatment protocol, we performed a p
Autor:
Anne Demulder, Laurence Rozen, Phu Quoc Lê, Alina Ferster, Denis F. Noubouossie, Mahadeb Bhavna, Malou Ngalula Mujinga, Dominique Willems
Publikováno v:
Blood. 120:4762-4762
Abstract 4762 Introduction: Abnormalities of the clotting system are often observed in sickle cell disease (SCD). In addition to activation of coagulation, increased thrombin generation (TG) has recently been demonstrated in SCD children Aim of the s
Autor:
Françoise Vertongen, Béatrice Gulbis, Ba-Cuong Nguyen, Christiane Vermylen, Anna Vanderfaeillie, André Efira, Malou Ngalula Mujinga, Catherine Heijmans, Alina Ferster, Phu Quoc Lê
Publikováno v:
Blood. 116:2659-2659
Abstract 2659 Sickle cell disease (SCD) has polymorphic manifestations, it is not well known by many physicians, and patients have often a precarious status. So despite enormous improvements in the understanding of the pathogenesis of SCD, patient ca
Autor:
Phu Quoc Lê, Hanane El Kenz, Michel Ntetani Aloni, Nadira Azzi, Alina Ferster, Catherine Heijmans, Sophie Huybrechts, Malou Ngalula Mujinga, Christine Devalck
Publikováno v:
Blood. 116:4821-4821
Abstract 4821 Background: Red cell exchange transfusion is frequently used in the management of patients with sickle cell disease either electively or therapeutically to maintain an hemoglobin S (Hb S) level < 30–50%. This target is often difficult
Autor:
Pauline Lecerf, Catherine Heijmans, Michel Ntetani Aloni, Alina Ferster, Sophie Huybrechts, Phu Quoc Lê, Christine Devalck, Malou Ngalula Mujinga
Publikováno v:
Blood. 116:4807-4807
Abstract 4807 Background: Pica defined as a compulsive and persistent intake of inedible substances or atypical food combinations at least one month. Association of pica and sickle cell disease (SCD) are poorly documented. Alerted by parents, we deci
Autor:
Dedeken, Laurence, Le, Phu-Quoc, Azzi, Nadira *, Brachet, Cecile *, Heijmans, Catherine *, Huybrechts, Sophie *, Devalck, Christine *, Malou, Ngalula Mujinga *, Ferster, Alina
Publikováno v:
In Blood 18 November 2011 118(21):3103-3103