UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Methylenetetrahydrofolate Reductase Gene A1298C Polymorphism in Pediatric Stroke—Case–Control and Family-based Study

Journal of stroke and cerebrovascular diseases, 2015, Vol.24 (1), p.61-65

2015

Volltextzugriff (PDF)

Assessment of clinical risk factors for drug-resistant epilepsy in children and teenagers

Studia medyczne, 2014-01, Vol.3 (3), p.141-147

2014

Volltextzugriff (PDF)

Nicolaides-Baraitser syndrome in the assessment of an interdisciplinary team

Studia medyczne, 2013-08, Vol.29 (2), p.180-184

2013

Volltextzugriff (PDF)

The effect of seizures on functional status of people with spastic forms of cerebral palsy

Journal of Epileptology, 2015-12, Vol.23 (2), p.91-102

2015

Volltextzugriff (PDF)

Associations between MDR1 C3435T polymorphism and drug-resistant epilepsy in the Polish population

Acta neurologica Belgica, 2017-03, Vol.117 (1), p.153-158

2017

Volltextzugriff (PDF)

Epilepsy and mental retardation. The school's functioning in children with epilepsy

Przeglad lekarski, 2010, Vol.67 (11), p.1175

Wendorff, Janusz

2010

Volltextzugriff (PDF)

The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study

Journal of stroke and cerebrovascular diseases, 2017-12, Vol.26 (12), p.2763-2768

2017

Volltextzugriff (PDF)

The diagnostic and therapeutic management in the first cerebral attack in childhood

Przeglad lekarski, 2007, Vol.64 Suppl 3, p.32

Wendorff, Janusz

2007

Volltextzugriff (PDF)

Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke

Journal of stroke and cerebrovascular diseases, 2018-07, Vol.27 (7), p.1885-1889

2018

Volltextzugriff (PDF)

The T Allele of the 677C>T Polymorphism of Methylenetetrahydrofolate Reductase Gene is Associated With an Increased Risk of Ischemic Stroke in Polish Children

Journal of child neurology, 2009-10, Vol.24 (10), p.1262-1267

2009

Volltextzugriff (PDF)

Polymorphisms of genes encoding coagulation factors II, V, VII, and XIII in relation to pediatric ischemic stroke: family-based and case-control study

The Neurologist (Baltimore, Md.), 2012-09, Vol.18 (5), p.282-286

2012

Volltextzugriff (PDF)

Photosensitivity in children with idiopathic headaches

Neurologia i neurochirurgia polska, 2005, Vol.39 (4 Suppl 1), p.S9

2005

Volltextzugriff (PDF)

Impact of the -174G/C interleukin-6 (IL-6) gene polymorphism on the risk of paediatric ischemic stroke, its symptoms and outcome

Folia neuropathologica, 2012, Vol.50 (2), p.147-151

2012

Volltextzugriff (PDF)

Lentigines in different multiple organ defects syndromes

Polski merkuriusz lekarski, 2009-01, Vol.26 (151), p.86

2009

Volltextzugriff (PDF)

Hypoxic-ischemic encephalopathy as a special form of head injury complication in battered child syndrome

Archiwum medycyny sądowej i krjminologii, 2010-04, Vol.60 (2-3), p.137

2010

Volltextzugriff (PDF)

Evaluation of brain activation by functional magnetic resonance in offspring of epileptic mothers and their parents in pathogenetic aspects of dyslexia

Przeglad lekarski, 2006, Vol.63 (12), p.1294

2006

Volltextzugriff (PDF)

Cognitive disturbances in rolandic epilepsy--correlation with electoencephalographic patterns

Przeglad lekarski, 2006, Vol.63 Suppl 1, p.14

2006

Volltextzugriff (PDF)

Pseudoatrophic macules as a additional skin sign of neurofibromatosis

Polski merkuriusz lekarski, 2007-03, Vol.22 (129), p.221

2007

Volltextzugriff (PDF)

Assessment of the communication difficulties of children and ado lescents with cerebral palsy using Communication Function Classification System

Child Neurology, 2018, Vol.27 (54), p.53-58

2018

Volltextzugriff (PDF)

Eating and drinking ability classification system in cerebral palsy

Neurologia dziecięca, 2017, Vol.26 (52), p.63-67

2017

Volltextzugriff (PDF)

The differential diagnosis of asymmetry in infants

Medycyna wieku rozwojowego, 2016, Vol.20 (4), p.335

2016

Volltextzugriff (PDF)

Neurocutaneous melanosis and congenital gigantic pigmented nevi in the light of current knowledge

Polski merkuriusz lekarski, 2005-01, Vol.18 (103), p.105

2005

Volltextzugriff (PDF)

Evaluation of EEG after long-lasting focal febrile seizures during childhood: prospective study until adulthood

Przeglad lekarski, 2003, Vol.60 Suppl 1, p.34

2003

Volltextzugriff (PDF)

Bickerstaff's brainstem encephalitis -- an analysis of clinical and MRI findings

Neurologia i neurochirurgia polska, 2006-01, Vol.40 (1), p.16

2006

Volltextzugriff (PDF)

Disorders of specific humoral immunological response in children with febrile seizures

Neurologia i neurochirurgia polska, 2004, Vol.38 (1 Suppl 1), p.S39

2004

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(11)

Publikationsform

Artikel
(29)

Sprache

Polnisch
(16)
Englisch
(14)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Methylenetetrahydrofolate Reductase Gene A1298C Polymorphism in Pediatric Stroke—Case–Control and Family-based Study

Assessment of clinical risk factors for drug-resistant epilepsy in children and teenagers

Nicolaides-Baraitser syndrome in the assessment of an interdisciplinary team

The effect of seizures on functional status of people with spastic forms of cerebral palsy

Associations between MDR1 C3435T polymorphism and drug-resistant epilepsy in the Polish population

Epilepsy and mental retardation. The school's functioning in children with epilepsy

The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study

The diagnostic and therapeutic management in the first cerebral attack in childhood

Upstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic Stroke

The T Allele of the 677C>T Polymorphism of Methylenetetrahydrofolate Reductase Gene is Associated With an Increased Risk of Ischemic Stroke in Polish Children

Polymorphisms of genes encoding coagulation factors II, V, VII, and XIII in relation to pediatric ischemic stroke: family-based and case-control study

Photosensitivity in children with idiopathic headaches

Impact of the -174G/C interleukin-6 (IL-6) gene polymorphism on the risk of paediatric ischemic stroke, its symptoms and outcome

Lentigines in different multiple organ defects syndromes

Hypoxic-ischemic encephalopathy as a special form of head injury complication in battered child syndrome

Evaluation of brain activation by functional magnetic resonance in offspring of epileptic mothers and their parents in pathogenetic aspects of dyslexia

Cognitive disturbances in rolandic epilepsy--correlation with electoencephalographic patterns

Pseudoatrophic macules as a additional skin sign of neurofibromatosis

Assessment of the communication difficulties of children and ado lescents with cerebral palsy using Communication Function Classification System

Eating and drinking ability classification system in cerebral palsy

The differential diagnosis of asymmetry in infants

Neurocutaneous melanosis and congenital gigantic pigmented nevi in the light of current knowledge

Evaluation of EEG after long-lasting focal febrile seizures during childhood: prospective study until adulthood

Bickerstaff's brainstem encephalitis -- an analysis of clinical and MRI findings

Disorders of specific humoral immunological response in children with febrile seizures

Suchergebnisse filtern