F.J.M Gabreëls: search on Z-Library

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1

Towards a standardised assessment procedure for developmental apraxia of speech

Geert Thoonen, Ben Maassen, F. Gabreëls, R. Schreuder, B. de Swart

Journal:

International Journal of Language & Communication Disorders

Year:

1997

Language:

english

File:

PDF, 1.60 MB

english, 1997

2

The Moya-Moya syndrome: A report of two children

van Erven, P.M.M., Gabreëls, F.J.M., Thijssen, H.O.M., Renier, W.O.

Journal:

Clinical Neurology and Neurosurgery

Year:

1982

Language:

english

File:

PDF, 945 KB

english, 1982

3

Spina Bifida and Parental Occupation

Blatter, Birgitte M., Roeleveld, Nel, Zielhuis, Gerhard A., Mullaart, Reinier A., Gabreëls, Fons J. M.

Journal:

Year:

1996

File:

PDF, 469 KB

1996

4

Building centres of expertise according to the Dutch model?

Fons JM Gabreëls, Jolanda S Huizer

Journal:

Orphanet Journal of Rare Diseases

Year:

2010

Language:

english

File:

PDF, 176 KB

english, 2010

5

A statistical approach to fiber diameter distribution in human sural nerve

Dr. Ronald L. L. A. Schellens, Dr. Benno K. van Veen, Dr. Annexe A. W. M. Gabreëls-Festen, Dr. Servaas L. H. Notermans, Dr. Martin A. van't Hof, Dr. Dick F. Stegeman

Journal:

Year:

1993

Language:

english

File:

PDF, 676 KB

english, 1993

6

Fasting studies in cerebrospinal fluid and blood in children with epilepsy of unknown origin

K.J.B. Lamers, F.J.M. Gabreëls, W.O. Renier, R.A. Wevers, W.H. Doesburg

Journal:

Epilepsy Research

Year:

1995

Language:

english

File:

PDF, 351 KB

english, 1995

7

Mutiple mucosal neuromas, dysautonomia and abnormal intradermal histamine reaction

Joosten, E.M.G., Gabreëls-Festen, A.W.M., Jaspar, H.H.J., van Haelst, U.J.G., Korten, J.J., Horstink, M.W.I.M., Gabreëls, F.J.M.

Journal:

Clinical Neurology and Neurosurgery

Year:

1974

Language:

english

File:

PDF, 1.43 MB

english, 1974

8

Planning of syllables in children with developmental apraxia of speech

Nijland, Lian, Maassen, Ben, van der Meulen, Sjoeke, Gabreëls, Fons, Kraaimaat, Floris W., Schreuder, Rob

Journal:

Clinical Linguistics & Phonetics

Year:

2003

Language:

english

File:

PDF, 517 KB

english, 2003

9

Cerebrotendinous xanthomatosis: Controversies about nerve and muscle: observations in ten patients

A Verrips, B.G.M van Engelen, H ter Laak, A Gabreëls-Festen, A Janssen, M Zwarts, R.A Wevers, F.J.M Gabreëls

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 574 KB

english, 2000

10

ASSESSMENT OF POST-TRAUMATIC AMNESIA IN YOUNG CHILDREN

M. B. M. Ruijs, A. Keyser, F. J. M. Gabreëls

Journal:

Developmental Medicine & Child Neurology

Year:

1992

Language:

english

File:

PDF, 595 KB

english, 1992

11

The Aicardi-Goutières syndrome: Variable clinical expression in two siblings

Aad Verrips, Johan A.P. Hiel, Fons J.M. Gabreëls, Pieter Wesseling, Jan J. Rotteveel

Journal:

Pediatric Neurology

Year:

1997

Language:

english

File:

PDF, 848 KB

english, 1997

12

Intramedullary Spinal Cord Abscess- A Case Report

Bartels, Ronald H. M. A., Gonera, Ed G., van der Spek, Johannes A. N., Thijssen, Henk O. M., Mullaart, Reinier A., Gabreels, Fons J. M.

Journal:

Year:

1995

File:

PDF, 597 KB

1995

13

Complex regional pain syndrome type I (RSD): Pathology of skeletal muscle and peripheral nerve

van der Laan, L., ter Laak, H. J., Gabreels-Festen, A., Gabreels, F., Goris, R.J.A.

Journal:

Year:

1998

Language:

english

File:

PDF, 1.01 MB

english, 1998

14

Sensory potentials and sural nerve biopsy: A Model evaluation

Dr. Ruurd Schoonhoven, Dr. Ronald L. L. A. Schellens, Dr. Dick F. Stegeman, Dr. Anneke A. W. M. Gabreëls-Festen

Journal:

Year:

1987

Language:

english

File:

PDF, 989 KB

english, 1987

15

Clinical features of Niemann-Pick disease type C an example of the delayed onset, slowly progressive phenotype and an overview of recent literature

van de Vlasakker, C.J.W., Gabreëls, F.J.M., Wijburg, H.C., Wevers, R.A.

Journal:

Clinical Neurology and Neurosurgery

Year:

1994

Language:

english

File:

PDF, 646 KB

english, 1994

16

Conduction velocity distributions compared to fiber size distributions in normal human sural nerve

Dr. Benno K. van Veen, Dr. Ronald L. L. A. Schellens, Dr. Dick F. Stegeman, Dr. Ruurd Schoonhoven, Dr. Anneke A. W. M. Gabreëls-Festen

Journal:

Year:

1995

Language:

english

File:

PDF, 591 KB

english, 1995

17

Familial adult-onset muscular dystrophy with leukoencephalopathy

Dr Baziel G. M. van Engelen, Quint H. Leyten, Pieter L. J. A. Bernsen, Fons J. M. Gabreëls, Ed M. G. Joosten, Henk J. ter Laak, Mechelien B. M. Ruijs, Ben C. J. Hamel, Johan R. M. Cruysberg, Frederik

Journal:

Annals of Neurology

Year:

1992

Language:

english

File:

PDF, 432 KB

english, 1992

18

Major histocompatibility complex class II expression and macrophage responses in genetically proven Charcot–Marie–Tooth type 1 and hereditary neuropathy with liability to pressure palsies

Guido Stoll, Anneke A.W.M. Gabreëls-Festen, Sebastian Jander, Hans-Werner Müller, C. Oliver Hanemann

Journal:

Year:

1998

Language:

english

File:

PDF, 1.02 MB

english, 1998

19

Recurrent neuropathy associated with Ehlers–Danlos syndrome

N. C. Voermans, G. Drost, A. van Kampen, A. A. Gabreëls–Festen, M. Lammens, B. C. Hamel, J. Schalkwijk, B. G. van Engelen

Journal:

Journal of Neurology

Year:

2006

Language:

english

File:

PDF, 164 KB

english, 2006

20

Validity of maximum performance tasks to diagnose motor speech disorders in children

G. THOONEN B. MAASSEN F. GABREELS R,

Journal:

Clinical Linguistics & Phonetics

Year:

1999

Language:

english

File:

PDF, 304 KB

english, 1999

21

Sjogren-Larsson syndrome: Clinical and MRI/MRS findings in FALDH-deficient patients

van Domburg, P. H. M. F., Willemsen, M. A. A. P., Rotteveel, J. J., de Jong, J. G. N., Thijssen, H. O. M., Heerschap, A., Cruysberg, J. R. M., Wanders, R. J. A., Gabreels, F. J. M., Steijlen, P. M.

Journal:

Year:

1999

Language:

english

File:

PDF, 1.53 MB

english, 1999

22

Maximum Performance Tests in Children With Developmental Spastic Dysarthria

Wit, J., Maassen, B., Gabreëls, F. J. M., Thoonen, G.

Journal:

Journal of Speech Language and Hearing Research

Year:

1993

Language:

english

File:

PDF, 769 KB

english, 1993

23

The syndrome of hypertension and hyperkalaemia with normal glomerular function (Gordon's syndrome)

B. Semmekrot, L. Monnens, B. G. A. Theelen, W. Rascher, F. Gabreëls, J. Willems

Journal:

Pediatric Nephrology

Year:

1987

Language:

english

File:

PDF, 489 KB

english, 1987

24

The integrated use of maximum performance tasks in differential diagnostic evaluations among children with motor speech disorders

Thoonen, G., Maassen, B., Wit, J., Gabreëls, F., Schreuder, R.

Journal:

Clinical Linguistics & Phonetics

Year:

1996

Language:

english

File:

PDF, 1.71 MB

english, 1996

25

Congenital muscular dystrophy and severe central nervous system atrophy in two siblings

Q. H. Leyten, P. G. Barth, F. J. M. Gabreëls, K. Renkawek, W. O. Renier, A. A. W. M. Gabreëls-Festen, H. J. ter Laak, M. G. Smits

Journal:

Acta Neuropathologica

Year:

1995

Language:

english

File:

PDF, 2.84 MB

english, 1995

26

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q

J. C. Fischer, W. Ruitenbeek, F. J. M. Gabreëls, A. J. M. Janssen, W. O. Renier, R. C. A. Sengers, A. M. Stadhouders, H. J. Laak, J. M. F. Trijbels, J. H. Veerkamp

Journal:

European Journal of Pediatrics

Year:

1986

Language:

english

File:

PDF, 1.00 MB

english, 1986

27

The concentration of blood components related to fuel metabolism during prolonged fasting in children

K.J.B. Lamers, W.H. Doesburg, F.J.M. Gabreëls, W.A.J.G. Lemmens, A.C. Romsom, R.A. Wevers, W.O. Renier

Journal:

Clinica Chimica Acta

Year:

1985

Language:

english

File:

PDF, 614 KB

english, 1985

28

Treatment of complex I deficiency with riboflavin

P.L.J.A. Bernsen, F.J.M. Gabreëls, W. Ruitenbeek, H.L. Hamburger

Journal:

Journal of the Neurological Sciences

Year:

1993

Language:

english

File:

PDF, 809 KB

english, 1993

29

Attenuation of the Polypeptide 7B2, Prohormone Convertase PC2, and Vasopressin in the Hypothalamus of Some Prader-Willi Patients: Indications for a Processing Defect

Gabreels, B. A. Th. F.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1998

Language:

english

File:

PDF, 1.04 MB

english, 1998

30

Cranio-vertebral pathology in Down syndrome

Braakhekke, J.P., Gabreëls, F.J.M., Renier, W.O., van Rens, T.J.G., Thijssen, H.O.M., Begeer, J.H.

Journal:

Clinical Neurology and Neurosurgery

Year:

1985

Language:

english

File:

PDF, 862 KB

english, 1985

31

Mental retardation and parential occupation: a study on the aetiology

Roeleveld, N., Zielhuis, G.A., Gabreëls, F.

Journal:

Clinical Neurology and Neurosurgery

Year:

1991

Language:

english

File:

PDF, 136 KB

english, 1991

32

Sporadic distal dystonia: A clinical study of seven juvenile cases

Busard, H.L.S.M., Renier, W.O., Gabreëls, F.J.M., Horstink, M.W.J.M., Rotteveel, J.J.

Journal:

Clinical Neurology and Neurosurgery

Year:

1983

Language:

english

File:

PDF, 1.08 MB

english, 1983

33

Long-term effects of melatonin on quality of life and sleep in haemodialysis patients (Melody study): a randomized controlled trial

Russcher, Marije, Koch, Birgit C. P., Nagtegaal, J. Elsbeth, van Ittersum, Frans J., Pasker-de Jong, Pieternel C. M., Hagen, E. Chris, van Dorp, Wim Th, Gabreëls, Bas, Wildbergh, Thierry X., van der W

Journal:

British Journal of Clinical Pharmacology

Year:

2013

Language:

english

File:

PDF, 1.03 MB

english, 2013

34

Cerebrotendinous Xanthomatosis: The Spectrum of Imaging Findings and the Correlation with Neuropathologic Findings1

Barkhof, Frederik, Verrips, Aad, Wesseling, Pieter, van der Knaap, Marjo S., van Engelen, Baziel G. M., Gabreëls, Fons J. M., Keyser, Antoine, Wevers, Ron A., Valk, Jaap

Journal:

Year:

2000

Language:

english

File:

PDF, 1.38 MB

english, 2000

35

Validity and reproducibility of the Jamar dynamometer in children aged 4 – 11 years

van den Beld, Willeke A., van den Beld, Willeke A., van der Sanden, Gitty A. C., Sengers, Rob C. A., Verbeek, André L. M., Gabreëls, Fons J. M.

Journal:

Disability & Rehabilitation

Year:

2006

Language:

english

File:

PDF, 135 KB

english, 2006

36

Attenuation of the Polypeptide 7B2, Prohormone Convertase PC2, and Vasopressin in the Hypothalamus of Some Prader-Willi Patients: Indications for a Processing Defect

Gabreëls, B. A. Th. F., Swaab, D. F., de Kleijn, D. P. V., Seidah, N. G., Van de Loo, J.-W., Van de Ven, W. J. M., Martens, G. J. M., van Leeuwen, F. W.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1998

Language:

english

File:

PDF, 1.03 MB

english, 1998

37

Inherited demyelinating peripheral neuropathies: Relating myelin packing abnormalities to P0 molecular defects

D.A. Kirschner, K. Szumowski, A.A.W.M. Gabreëls-Festen, J.E. Hoogendijk, P.A. Bolhuis

Journal:

Journal of Neuroscience Research

Year:

1996

Language:

english

File:

PDF, 1013 KB

english, 1996

38

Pyruvate carboxylase activity is not abnormal in fibroblasts of patients with Friedreich's ataxia

U. J. Dijkstra, J. M. F. Trijbels, W. Ruitenbeek, J. A. J. M. Bakkeren, A. J. M. Janssen, F. J. M. Gabreëls, E. M. G. Joosten

Journal:

Annals of Neurology

Year:

1984

Language:

english

File:

PDF, 105 KB

english, 1984

39

Friedreich ataxia and low pyruvate carboxylase activity in liver and fibroblasts

U. J. Dijkstra, J. L. Willems, Dr E. M. G. Joosten, F. J. M. Gabreëls

Journal:

Annals of Neurology

Year:

1983

Language:

english

File:

PDF, 386 KB

english, 1983

40

A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome

D. Daniëlle de Vries, Baziel G. M. van Engelen, Fons J. M. Gabreëls, Wim Ruitenbeek, Dr. Bernard A. van Oost

Journal:

Annals of Neurology

Year:

1993

Language:

english

File:

PDF, 303 KB

english, 1993

41

Hyperkalemic periodic paralysis in Gordon's syndrome: A possible defect in atrial natriretic peptide function

J. W. Pasman, Dr F. J. M. Gabreëls, B. Semmekrot, W. O. Renier, L. A. H. Monnens

Journal:

Annals of Neurology

Year:

1989

Language:

english

File:

PDF, 495 KB

english, 1989

42

An autosomal dominant type of congenital muscular dystrophy

Leyten, Quint H, Gabreëls, Fons JM, Joosten, Ed MG, Renier, Willy O, Ter Laak, Henk J, Ter Haar, Ben GA, Stadhouders, Ad M

Journal:

Brain and Development

Year:

1986

Language:

english

File:

PDF, 1.18 MB

english, 1986

43

GM2-gangliosidosis

Praamstra, P., Wevers, R.A., Gabreëls, F.J.M., Rotteveel, J.J., Renier, W.O., Sengers, R.C.A., Lamers, K.J.B.

Journal:

Clinical Neurology and Neurosurgery

Year:

1990

Language:

english

File:

PDF, 619 KB

english, 1990

44

A new leukoencephalopathy with vanishing white matter

van der Knaap, M. S., Barth, P. G., Gabreels, F.J.M., Franzoni, E., Begeer, J. H., Stroink, H., Rotteveel, J. J., Valk, J.

Journal:

Year:

1997

Language:

english

File:

PDF, 1.30 MB

english, 1997

45

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Azzedine, H., Ravise, N., Verny, C., Gabreels-Festen, A., Lammens, M., Grid, D., Vallat, J. M., Durosier, G., Senderek, J., Nouioua, S., Hamadouche, T., Bouhouche, A., Guilbot, A., Stendel, C., Ruberg

Journal:

Year:

2006

Language:

english

File:

PDF, 386 KB

english, 2006

46

Left Ventricular Diastolic Dysfunction in Dialysis Patients Assessed by Novel Speckle Tracking Strain Rate Analysis: Prevalence and Determinants

de Bie, Mihály K., Ajmone Marsan, Nina, Gaasbeek, André, Bax, Jeroen J., Groeneveld, Marc, Gabreels, Bas A., Delgado, Victoria, Rabelink, Ton J., Schalij, Martin J., Jukema, J. Wouter

Journal:

International Journal of Nephrology

Year:

2012

Language:

english

File:

PDF, 636 KB

english, 2012

47

Occupational Exposure and Defects of the Central Nervous System in Offspring: Review

N. Roeleveld, G. A. Zielhuis and F. Gabreëls

Journal:

British Journal of Industrial Medicine

Year:

1990

Language:

english

File:

PDF, 1.84 MB

english, 1990

48

Disturbances of Cerebral Purine and Pyrimidine Metabolism in Young Children with Chronic Renal Failure

Gerrits, G.P.J.M., Monnens, L.A.H., DeAbreu, R.A., Schröder, C.H., Trijbels, J.M.F., Gabreëls, F.J.M.

Journal:

Year:

1991

Language:

english

File:

PDF, 833 KB

english, 1991

49

Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies

Peter H. S. Meijerink, Ina Zorn, Frank Baas, Marianne de Visser, Dr Pieter A. Bolhuis, Jessica E. Hoogendijk, Henk Veldman, Anneke A. W. M. Gabreëls-Festen

Journal:

Annals of Neurology

Year:

1996

Language:

english

File:

PDF, 440 KB

english, 1996

50

Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies

E. C. M. Mariman, A. A. W. M. Gabreëls-Festen, S. E. C. Beersum, P. J. H. Jongen, E. Looij, F. Baas, P. A. Bolhuis, H. H. Ropers, F. J. M. Gabreëls

Journal:

Year:

1994

Language:

english

File:

PDF, 624 KB

english, 1994

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