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Eyskens, F.
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1

Expérience des patients Fabry concernant la perfusion mensu..:

Eyskens, F. ; Ankit, M. ; Pisani, A....
La Revue de Médecine Interne.  45 (2024)  - p. A142-A143 , 2024
Link: https://doi.org/10.1016/..
 
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2

P001 Cystic fibrosis newborn screening (CF-NBS) start-up in..:

Proesmans, M. ; Regal, L. ; Eyskens, F....
Journal of Cystic Fibrosis.  21 (2022)  - p. S61 , 2022
Link: https://doi.org/10.1016/..
 
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3

P011 Cystic fibrosis – newborn screening (CF-NBS) start-up ..:

Proesmans, M. ; Régal, L. ; Eyskens, F....
Journal of Cystic Fibrosis.  20 (2021)  - p. S41-S42 , 2021
Link: https://doi.org/10.1016/..
 
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4

The natural history of classic galactosemia: lessons from t..:

Rubio-Gozalbo, M. E. ; Haskovic, M. ; Bosch, A. M....
Orphanet Journal of Rare Diseases.  14 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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5

Dietary practices in propionic acidemia: A European survey:

Daly, A. ; Pinto, A. ; Evans, S....
Molecular Genetics and Metabolism Reports.  13 (2017)  - p. 83-89 , 2017
Link: https://doi.org/10.1016/..
 
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6

Dietary practices in isovaleric acidemia: A European survey:

Pinto, A. ; Daly, A. ; Evans, S....
Molecular Genetics and Metabolism Reports.  12 (2017)  - p. 16-22 , 2017
Link: https://doi.org/10.1016/..
 
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7

Can psychiatric childhood disorders be due to inborn errors..:

Simons, A. ; Eyskens, F. ; Glazemakers, I..
European Child & Adolescent Psychiatry.  26 (2016)  2 - p. 143-154 , 2016
Link: https://doi.org/10.1007/..
 
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8

An international, phase 3, switchover study of reveglucosid..:

Schoser, B. ; Byrne, B. ; Eyskens, F....
Neuromuscular Disorders.  25 (2015)  - p. S189 , 2015
Link: https://doi.org/10.1016/..
 
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9

Dietary practices in pyridoxine non-responsive homocystinur..:

Adam, S. ; Almeida, M.F. ; Carbasius Weber, E....
Molecular Genetics and Metabolism.  110 (2013)  4 - p. 454-459 , 2013
Link: https://doi.org/10.1016/..
 
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10

Dietary management of urea cycle disorders: European practi..:

Adam, S. ; Almeida, M.F. ; Assoun, M....
Molecular Genetics and Metabolism.  110 (2013)  4 - p. 439-445 , 2013
Link: https://doi.org/10.1016/..
 
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11

Fabry disease: a review of current management strategies:

Mehta, A. ; Beck, M. ; Eyskens, F....
QJM.  103 (2010)  9 - p. 641-659 , 2010
Link: https://doi.org/10.1093/..
 
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12

Fabry disease in a patient with Turner syndrome:

Brouns, R. ; Eyskens, F. ; De Boeck, K....
Journal of Inherited Metabolic Disease.  32 (2009)  S1 - p. 45-48 , 2009
Link: https://doi.org/10.1007/..
 
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13

G.P.10 10 Newborn screening for Duchenne muscular dystrophy..:

Eyskens, F. ; Philips, E.
Neuromuscular Disorders.  16 (2006)  9-10 - p. 721 , 2006
Link: https://doi.org/10.1016/..
 
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14

Multiplex ligation‐dependent probe amplification to detect ..:

Rooms, L ; Reyniers, E ; Wuyts, W...
Clinical Genetics.  69 (2005)  1 - p. 58-64 , 2005
Link: https://doi.org/10.1111/..
 
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15

Unusual enzyme findings in five patients with metabolic pro..:

Gibson, K. M. ; Sweetman, L. ; Kozich, V....
Journal of Inherited Metabolic Disease.  21 (1998)  3 - p. 255-261 , 1998
Link: https://doi.org/10.1023/..
 
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