FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Vincent Ramaekers

Research Profile

Living Beings

Concepts & Ideas

Chemicals & Drugs

Disorders

Physiology

Phenotype

Anatomy

Myelinated Nerve Fibers

Co-author Network

Publications

TOP 3
Jeffrey M Sequeira; Vincent T Ramaekers; Edward V Quadros
The diagnostic utility of folate receptor autoantibodies in blood.
Vincent T Ramaekers; Jeffrey M Sequeira; Edward V Quadros
Clinical recognition and aspects of the cerebral folate deficiency syndromes.
Vincent T Ramaekers; J Weis; Jeffrey M Sequeira; Edward V Quadros; Nenad Blau
Mitochondrial complex I encephalomyopathy and cerebral 5-methyltetrahydrofolate deficiency.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Vincent Ramaekers (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Jeffrey M Sequeira; Vincent T Ramaekers; Edward V Quadros
The diagnostic utility of folate receptor autoantibodies in blood.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2013;51(3):545-54.
2013: Vincent T Ramaekers; Jeffrey M Sequeira; Edward V Quadros
Clinical recognition and aspects of the cerebral folate deficiency syndromes.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2013;51(3):497-511.
2007: Vincent T Ramaekers; J Weis; Jeffrey M Sequeira; Edward V Quadros; Nenad Blau
Mitochondrial complex I encephalomyopathy and cerebral 5-methyltetrahydrofolate deficiency.
Neuropediatrics 2007;38(4):184-7.
2007: Vincent T Ramaekers; Jeffrey M Sequeira; Rafael Artuch; Nenad Blau; T Temudo; Aida Ormazabal; Manuel Pineda; Asun Aracil; F Roelens; Franco Laccone; Edward V Quadros
Folate receptor autoantibodies and spinal fluid 5-methyltetrahydrofolate deficiency in Rett syndrome.
Neuropediatrics 2007;38(4):179-83.
2006: Thomas Opladen; Vincent T Ramaekers; Gerhard Heimann; Nenad Blau
Analysis of 5-methyltetrahydrofolate in serum of healthy children.
Molecular genetics and metabolism 2006;87(1):61-5.
2005: Vincent T Ramaekers; Sheldon P Rothenberg; Jeffrey M Sequeira; Thomas Opladen; Nenad Blau; Edward V Quadros; Jacob Selhub
Autoantibodies to folate receptors in the cerebral folate deficiency syndrome.
The New England journal of medicine 2005;352(19):1985-91.
2005: Martin Häusler; D Anhuf; Herdit Schüler; Vincent T Ramaekers; Armin Thron; Klaus Zerres; Walter Möller-Hartmann
White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelination.
Neuroradiology 2005;47(1):83-6.
2004: Vincent T Ramaekers; Nenad Blau
Cerebral folate deficiency.
Developmental medicine and child neurology 2004;46(12):843-51.
2004: Martin Häusler; Ulrich Merz; C Van Tuil; Vincent T Ramaekers
Long-term outcome after neonatal parenchymatous brain lesions.
Klinische Pädiatrie 2004;216(4):244-51.
2004: Marcus C Korinth; Vincent T Ramaekers; Veit Rohde
Cervical cord exostosis compressing the axis in a boy with hereditary multiple exostoses. Case illustration.
Journal of neurosurgery 2004;100(2 Suppl Pediatrics):223.
2003: Nenad Blau; Luisa Bonafé; I Krägeloh-Mann; Beat Thöny; Lucja Kierat; M Häusler; Vincent T Ramaekers
Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: a new phenotype.
Neurology 2003;61(5):642-7.
2003: Vincent T Ramaekers; Steen Ingemann Hansen; Jan Holm; Thomas Opladen; Jan Senderek; Martin Häusler; Gerhard Heimann; B Fowler; R Maiwald; Nenad Blau
Reduced folate transport to the CNS in female Rett patients.
Neurology 2003;61(4):506-15.
2003: Carsten Bergmann; Klaus Zerres; Jan Senderek; Sabine Rudnik-Schoneborn; Thomas Eggermann; Martin Häusler; Michael Mull; Vincent T Ramaekers
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia.
Brain : a journal of neurology 2003;126(Pt 7):1537-44.
2003: Martin Häusler; Lars Schaade; Vincent T Ramaekers; Martin Doenges; Gerhard Heimann; Bernd Sellhaus
Inflammatory pseudotumors of the central nervous system: report of 3 cases and a literature review.
Human pathology 2003;34(3):253-62.
2003: Jan Senderek; Carsten Bergmann; Vincent T Ramaekers; Eva Nelis; Günther Bernert; Astrid Makowski; Stephan Zuchner; Peter De Jonghe; Sabine Rudnik-Schöneborn; Klaus Zerres; J Michael Schröder
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy.
Brain : a journal of neurology 2003;126(Pt 3):642-9.
2003: Martin Häusler; Bernd Sellhaus; Klaus Schweizer; Vincent T Ramaekers; Thomas Opladen; Michael Kleines
Flow cytometric cerebrospinal fluid analysis in children.
Pathology, research and practice 2003;199(10):667-75.
2002: Vincent T Ramaekers; Martin Häusler; Thomas Opladen; Gerhard Heimann; Nenad Blau
Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: a novel neurometabolic condition responding to folinic acid substitution.
Neuropediatrics 2002;33(6):301-8.
2002: Martin Häusler; Vincent T Ramaekers; Martin Doenges; Klaus Schweizer; Klaus Ritter; Lars Schaade
Neurological complications of acute and persistent Epstein-Barr virus infection in paediatric patients.
Journal of medical virology 2002;68(2):253-63.
2002: Martin Häusler; Lars Schaade; S Kemény; Klaus Schweizer; C Schoenmackers; Vincent T Ramaekers
Encephalitis related to primary varicella-zoster virus infection in immunocompetent children.
Journal of the neurological sciences 2002;195(2):111-6.
2002: Joerg Schefels; Tobias G Wenzl; Ulrich Merz; Vincent T Ramaekers; Josef Holzki; Sabine Rudnik-Schoeneborn; Benita Hermanns; Helmut Hörnchen
Functional upper airway obstruction in a child with Freeman-Sheldon syndrome.
ORL; journal for oto-rhino-laryngology and its related specialties 2002;64(1):53-6.
2001: Jan Senderek; Vincent T Ramaekers; K Zerres; Sabine Rudnik-Schöneborn; J M Schröder; Carsten Bergmann
Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain.
Journal of the neurological sciences 2001;192(1-2):49-51.
2001: Martin Häusler; J Jaeken; E Mönch; Vincent T Ramaekers
Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: report on two siblings.
Neuropediatrics 2001;32(4):191-5.
2001: Vincent T Ramaekers; Jan Senderek; Martin Häusler; M Häring; N Abeling; Klaus Zerres; Carsten Bergmann; Gerhard Heimann; Nenad Blau
A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopa.
Molecular genetics and metabolism 2001;73(2):179-87.
2000: Catherine Disselhorst-Klug; Jörg Bahm; Vincent T Ramaekers; A Trachterna; Günter Rau
Non-invasive approach of motor unit recording during muscle contractions in humans.
European journal of applied physiology 2000;83(2-3):144-50.
2000: Harald D Müller; M Mugler; Vincent T Ramaekers; J Michael Schröder
Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy (HMSN-ADM).
Journal of the peripheral nervous system : JPNS 2000;5(3):147-57.
1999: Jan Senderek; B Hermanns; Carsten Bergmann; Babak Boroojerdi; Malek Bajbouj; Marcel Hungs; Vincent T Ramaekers; S Quasthoff; D Karch; J Michael Schröder
X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1).
Journal of the neurological sciences 1999;167(2):90-101.
1998: Martin Häusler; Vincent T Ramaekers; J Reul; R Meilicke; Gerhard Heimann
Early and late onset manifestations of cerebral vasculitis related to varicella zoster.
Neuropediatrics 1998;29(4):202-7.
1998: Jan Senderek; Carsten Bergmann; S Quasthoff; Vincent T Ramaekers; J Michael Schröder
X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln).
Acta neuropathologica 1998;95(5):443-9.
1997: Vincent T Ramaekers; Gerhard Heimann; J Reul; A Thron; J Jaeken
Genetic disorders and cerebellar structural abnormalities in childhood.
Brain : a journal of neurology 1997;120 ( Pt 10)():1739-51.
1997: Vincent T Ramaekers; B Bosman; Gerbert Jansen; R J Wanders
Increased plasma malondialdehyde associated with cerebellar structural defects.
Archives of disease in childhood 1997;77(3):231-4.
1997: Vincent T Ramaekers; J Reul; G Kusenbach; A Thron; Gerhard Heimann
Central pontine myelinolysis associated with acquired folate depletion.
Neuropediatrics 1997;28(2):126-30.
1997: J Weis; J Reul; Lothar Mayfrank; Vincent T Ramaekers; Armin Thron
Duplication of a vertebral artery associated with epidermoid cyst of the posterior fossa.
European radiology 1997;7(3):412-4.
1995: Terttu Suormala; Vincent T Ramaekers; S Schweitzer; Brian Fowler; M C Laub; C Schwermer; J Bachmann; E Regula Baumgartner
Biotinidase Km-variants: detection and detailed biochemical investigations.
Journal of inherited metabolic disease 1995;18(6):689-700.
1994: Vincent T Ramaekers; J Reul; V Siller; Armin Thron
Mesencephalic and third ventricle cysts: diagnosis and management in four cases.
Journal of neurology, neurosurgery, and psychiatry 1994;57(10):1216-20.
1993: J Michael Schröder; G Heide; Vincent T Ramaekers; Wilhelm Mortier
Subtotal aplasia of myelinated nerve fibers in the sural nerve.
Neuropediatrics 1993;24(5):286-91.
1993: J Reul; Vincent T Ramaekers; Armin Thron
[Suprasellar space-occupying lesion as initial manifestation of tuberculosis in childhood].
Deutsche medizinische Wochenschrift (1946) 1993;118(22):820-4.
1993: Vincent T Ramaekers; Catherine Disselhorst-Klug; J Schneider; Jiri Silny; Juergen Forst; Raimund Forst; F Kotlarek; Günter Rau
Clinical application of a noninvasive multi-electrode array EMG for the recording of single motor unit activity.
Neuropediatrics 1993;24(3):134-8.
1993: Vincent T Ramaekers; M Brab; Günter Rau; Gerhard Heimann
Recovery from neurological deficits following biotin treatment in a biotinidase Km variant.
Neuropediatrics 1993;24(2):98-102.
1993: Jaak Jaeken; P De Cock; H Stibler; Chris Van Geet; J Kint; Vincent T Ramaekers; Hubert A Carchon
Carbohydrate-deficient glycoprotein syndrome type II.
Journal of inherited metabolic disease 1993;16(6):1041.
1992: M Brab; Vincent T Ramaekers; E Regula Baumgartner; Gerhard Heimann; Martin Reim
[Juvenile optic neuropathy caused by Km variants of biotinidase].
Klinische Monatsblätter für Augenheilkunde 1992;200(3):204-9.
1992: Vincent T Ramaekers; Terttu Suormala; M Brab; R Duran; Gerhard Heimann; E Regula Baumgartner
A biotinidase Km variant causing late onset bilateral optic neuropathy.
Archives of disease in childhood 1992;67(1):115-9.
1991: Vincent T Ramaekers; H Stibler; J Kint; Jaak Jaeken
A new variant of the carbohydrate deficient glycoproteins syndrome.
Journal of inherited metabolic disease 1991;14(3):385-8.
1990: Vincent T Ramaekers; P Casaer
Defective regulation of cerebral oxygen transport after severe birth asphyxia.
Developmental medicine and child neurology 1990;32(1):56-62.