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...

An 11-Year Follow-up Study of Neonatal-Onset, Bath-Induced Alternating Hemiplegia of Childhood in Twins

Journal of Child Neurology, 2012-05, Vol.27 (5), p.657-662

2012

Volltextzugriff (PDF)

Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications

International Journal of Endocrinology, 2014-01, Vol.2014 (2014), p.410-424-043

2014

Volltextzugriff (PDF)

Aicardi–Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations

Journal of pediatric neurology, 2020-08, Vol.18 (4), p.206-209

2020

Volltextzugriff (PDF)

Aicardi syndrome with multiple tumors: a case report with literature review

Brain & development (Tokyo. 1979), 1995-07, Vol.17 (4), p.283-285

1995

Volltextzugriff (PDF)

An animal model of maternal antibody-mediated arthrogryposis multiplex congenita (AMC)

Annals of the New York Academy of Sciences, 1998-05, Vol.841, p.565-567

1998

Volltextzugriff (PDF)

An Animal Model of Maternal Antibodymediated Arthrogryposis Multiplex Congenita (AMC)

Annals of the New York Academy of Sciences, 1998-05, Vol.841 (1), p.565-567

1998

Volltextzugriff (PDF)

Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia

Journal of pediatric neurology, 2024-05

2024

Volltextzugriff (PDF)

Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis

Journal of pediatric neurology, 2024-05

2024

Volltextzugriff (PDF)

Anomalies of the Craniocervical Junction (Chiari Malformations)

Journal of pediatric neurology, 2024-05

2024

Volltextzugriff (PDF)

Anomalies of the Mesenchyme (Meninges and Skull)—Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas; Arachnoid Cysts; Nonsyndromic and Syndromic Craniosynostoses

Journal of pediatric neurology, 2024-04, Vol.22 (2), p.114-124

2024

Volltextzugriff (PDF)

Another "new" form, the Palagonia type of acrofacial dysostosis in Sicilian family

American journal of medical genetics, 1997-04, Vol.69 (4), p.388-394

1997

Volltextzugriff (PDF)

Antibodies Affecting Ion Channel Function in Acquired Neuromyotonia, in Seropositive and Seronegative Myasthenia Gravis, and in Antibody-mediated Arthrogryposis Multiplex Congenita

Annals of the New York Academy of Sciences, 1998-05, Vol.841 (1), p.482-496

1998

Volltextzugriff (PDF)

Antibodies in Myasthenia Gravis and Related Disorders

Annals of the New York Academy of Sciences, 2003-09, Vol.998 (1), p.324-335

2003

Volltextzugriff (PDF)

Antibodies specific for fetal AChR induce arthrogryposis multiplex congenita in developing mice: an animal model for transfer of pathogenic antibodies

Journal of reproductive immunology, 1997, Vol.34 (1), p.95-96

1997

Volltextzugriff (PDF)

Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders

Journal of pediatric neurology, 2018-10, Vol.16 (5), p.255-264

2018

Volltextzugriff (PDF)

At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation

Journal of pediatric neurology, 2024-04, Vol.22 (2), p.96-107

2024

Volltextzugriff (PDF)

At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System

Journal of pediatric neurology, 2024-04, Vol.22 (2), p.108-113

2024

Volltextzugriff (PDF)

Ataxia-Telangiectasia

Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes, p.731-758

Volltextzugriff (PDF)

Autoimmune thyroiditis and acquired demyelinating polyradiculoneuropathy

Clinical neurology and neurosurgery, 2001-10, Vol.103 (3), p.151-154

2001

Volltextzugriff (PDF)

Becker's Nevus Syndrome

Journal of pediatric neurology, 2018-10, Vol.16 (5), p.352-361

2018

Volltextzugriff (PDF)

Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1

American journal of medical genetics. Part A, 2011-03, Vol.155 (3), p.582-585

2011

Volltextzugriff (PDF)

Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1

American Journal of Medical Genetics Part A, 2011, Vol.155A (3), p.582-585

2011

Volltextzugriff (PDF)

Bilateral Periventricular Nodular Heterotopia with Amniotic Band Syndrome

Pediatric neurology, 2007-06, Vol.36 (6), p.407-410

2007

Volltextzugriff (PDF)

Blue Rubber Bleb Nevus Syndrome

Journal of pediatric neurology, 2018-10, Vol.16 (5), p.288-296

2018

Volltextzugriff (PDF)

Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1 -hamartin" phenotype characterized by reduced cell growth

Frontiers in pediatrics, 2023-03, Vol.11, p.1101026

2023

Volltextzugriff (PDF)

1 – 25 von 164

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(149)
Mit Volltextzugriff
(102)

Publikationsform

Sprache

Englisch
(163)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

An 11-Year Follow-up Study of Neonatal-Onset, Bath-Induced Alternating Hemiplegia of Childhood in Twins

Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications

Aicardi–Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations

Aicardi syndrome with multiple tumors: a case report with literature review

An animal model of maternal antibody-mediated arthrogryposis multiplex congenita (AMC)

An Animal Model of Maternal Antibodymediated Arthrogryposis Multiplex Congenita (AMC)

Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia

Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis

Anomalies of the Craniocervical Junction (Chiari Malformations)

Anomalies of the Mesenchyme (Meninges and Skull)—Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas; Arachnoid Cysts; Nonsyndromic and Syndromic Craniosynostoses

Another "new" form, the Palagonia type of acrofacial dysostosis in Sicilian family

Antibodies Affecting Ion Channel Function in Acquired Neuromyotonia, in Seropositive and Seronegative Myasthenia Gravis, and in Antibody-mediated Arthrogryposis Multiplex Congenita

Antibodies in Myasthenia Gravis and Related Disorders

Antibodies specific for fetal AChR induce arthrogryposis multiplex congenita in developing mice: an animal model for transfer of pathogenic antibodies

Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders

At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation

At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System

Ataxia-Telangiectasia

Autoimmune thyroiditis and acquired demyelinating polyradiculoneuropathy

Becker's Nevus Syndrome

Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1

Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1

Bilateral Periventricular Nodular Heterotopia with Amniotic Band Syndrome

Blue Rubber Bleb Nevus Syndrome

Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1 -hamartin" phenotype characterized by reduced cell growth

Suchergebnisse filtern