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...

The Utility of Early Brain MRI for Patients with Neurofibromatosis Type 1 and Optic Pathway Glioma: A Long-Term Follow-Up in a Tertiary Referral Hospital

Neuropediatrics, 2022-10, Vol.53 (5), p.370-375

2022

Volltextzugriff (PDF)

Migraine abortive treatment in children and adolescents in Israel

Scientific reports, 2022-05, Vol.12 (1), p.7418-6, Article 7418

2022

Volltextzugriff (PDF)

Handwriting in children with Attention Deficient Hyperactive Disorder: role of graphology

BMC pediatrics, 2019-12, Vol.19 (1), p.484-484, Article 484

2019

Volltextzugriff (PDF)

Behavioral Symptoms May Correlate With the Load and Spatial Location of Tubers and With Radial Migration Lines in Tuberous Sclerosis Complex

Frontiers in neurology, 2021-10, Vol.12, p.673583-673583

2021

Volltextzugriff (PDF)

Optic Nerve Drusen Is Highly Prevalent Among Children With Pseudotumor Cerebri Syndrome

Frontiers in neurology, 2021-12, Vol.12, p.789673-789673

2021

Volltextzugriff (PDF)

Use of Optical Coherence Tomography to Detect Retinal Nerve Fiber Loss in Children With Optic Pathway Glioma

Frontiers in neurology, 2018-12, Vol.9, p.1102-1102

2018

Volltextzugriff (PDF)

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Neuromuscular disorders : NMD, 2017-02, Vol.27 (2), p.136-140

2017

Volltextzugriff (PDF)

Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri

Brain sciences, 2023-02, Vol.13 (2), p.361

2023

Volltextzugriff (PDF)

Children's Sleep Disturbance Scale in Differentiating Neurological Disorders

Pediatric neurology, 2013-12, Vol.49 (6), p.465-468

2013

Volltextzugriff (PDF)

High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome

Children (Basel), 2023-06, Vol.10 (7), p.1122

2023

Volltextzugriff (PDF)

Thick Corpus Callosum in Children

Journal of Clinical Neurology, 2017, 13(2), , pp.170-174

2017

Volltextzugriff (PDF)

Rolandic Epilepsy – A Silent Enemy. An Instructive Case

Curēus (Palo Alto, CA), 2021-07

2021

Volltextzugriff (PDF)

Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec –routine care evidence

Gene therapy, 2023-02, Vol.30 (1-2), p.101-106

2023

Volltextzugriff (PDF)

Giant Cystic Lesion in Neurofibromatosis

Pediatric neurology, 2009-12, Vol.41 (6), p.445-447

2009

Volltextzugriff (PDF)

Familial Benign Neonatal Sleep Myoclonus

Pediatric neurology, 2007-05, Vol.36 (5), p.334-337

2007

Volltextzugriff (PDF)

Prevalence of Epilepsy and Attention-Deficit Hyperactivity (ADHD) Disorder: A Population-Based Study

Journal of child neurology, 2013-01, Vol.28 (1), p.120-123

2013

Volltextzugriff (PDF)

Prognostic Parameters of Acute Transverse Myelitis in Children

Journal of child neurology, 2020-12, Vol.35 (14), p.999-1003

2020

Volltextzugriff (PDF)

Impairments in communication and social interaction in children with neurofibromatosis type 1: Characteristics and role of ADHD and language delay

Applied neuropsychology. Child, 2022-07, Vol.11 (3), p.220-225

2022

Volltextzugriff (PDF)

Trametinib for orbital plexiform neurofibromas in young children with neurofibromatosis type 1

Child's nervous system, 2021-06, Vol.37 (6), p.1909-1915

2021

Volltextzugriff (PDF)

Impact of a national population-based carrier-screening program on spinal muscular atrophy births

Neuromuscular disorders : NMD, 2020-12, Vol.30 (12), p.970-974

2020

Volltextzugriff (PDF)

Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing

European journal of human genetics : EJHG, 2016-11, Vol.24 (11), p.1635-1638

2016

Volltextzugriff (PDF)

Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years

Neuropediatrics, 2020-12, Vol.51 (6), p.440-444

2020

Volltextzugriff (PDF)

NFB-03. TRAMETINIB FOR ORBITAL PLEXIFORM NEUROFIBROMAS IN YOUNG CHILDREN WITH NF1

Neuro-oncology (Charlottesville, Va.), 2020-12, Vol.22 (Supplement_3), p.iii418-iii418

2020

Volltextzugriff (PDF)

Attention Deficit Hyperactivity Disorder in Neurofibromatosis Type 1: Evaluation with a Continuous Performance Test

Journal of Clinical Neurology, 2018, 14(2), , pp.153-157

2018

Volltextzugriff (PDF)

The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complex

Clinical genetics, 2020-02, Vol.97 (2), p.296-304

2020

Volltextzugriff (PDF)

1 – 25 von 92

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(83)
Mit Volltextzugriff
(79)

Publikationsform

Sprache

Englisch
(90)
Hebräisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

The Utility of Early Brain MRI for Patients with Neurofibromatosis Type 1 and Optic Pathway Glioma: A Long-Term Follow-Up in a Tertiary Referral Hospital

Migraine abortive treatment in children and adolescents in Israel

Handwriting in children with Attention Deficient Hyperactive Disorder: role of graphology

Behavioral Symptoms May Correlate With the Load and Spatial Location of Tubers and With Radial Migration Lines in Tuberous Sclerosis Complex

Optic Nerve Drusen Is Highly Prevalent Among Children With Pseudotumor Cerebri Syndrome

Use of Optical Coherence Tomography to Detect Retinal Nerve Fiber Loss in Children With Optic Pathway Glioma

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri

Children's Sleep Disturbance Scale in Differentiating Neurological Disorders

High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome

Thick Corpus Callosum in Children

Rolandic Epilepsy – A Silent Enemy. An Instructive Case

Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec –routine care evidence

Giant Cystic Lesion in Neurofibromatosis

Familial Benign Neonatal Sleep Myoclonus

Prevalence of Epilepsy and Attention-Deficit Hyperactivity (ADHD) Disorder: A Population-Based Study

Prognostic Parameters of Acute Transverse Myelitis in Children

Impairments in communication and social interaction in children with neurofibromatosis type 1: Characteristics and role of ADHD and language delay

Trametinib for orbital plexiform neurofibromas in young children with neurofibromatosis type 1

Impact of a national population-based carrier-screening program on spinal muscular atrophy births

Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing

Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years

NFB-03. TRAMETINIB FOR ORBITAL PLEXIFORM NEUROFIBROMAS IN YOUNG CHILDREN WITH NF1

Attention Deficit Hyperactivity Disorder in Neurofibromatosis Type 1: Evaluation with a Continuous Performance Test

The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complex

Suchergebnisse filtern