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...

Brain Symptoms of Tuberous Sclerosis Complex: Pathogenesis and Treatment

International journal of molecular sciences, 2021-06, Vol.22 (13), p.6677

2021

Volltextzugriff (PDF)

Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes

Brain & development (Tokyo. 1979), 2012-05, Vol.34 (5), p.337-343

2012

Volltextzugriff (PDF)

Comprehensive behavioral analysis of the Cdkl5 knockout mice revealed significant enhancement in anxiety- and fear-related behaviors and impairment in both acquisition and long-term retention of spatial reference memory

PloS one, 2018-04, Vol.13 (4), p.e0196587-e0196587

2018

Volltextzugriff (PDF)

GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion

Scientific reports, 2022-01, Vol.12 (1), p.1332-1332, Article 1332

2022

Volltextzugriff (PDF)

A severity score for acute necrotizing encephalopathy

Brain & development (Tokyo. 1979), 2015-03, Vol.37 (3), p.322-327

2015

Volltextzugriff (PDF)

Association of IL-1B rs16944 Polymorphism With Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion Is Opposite to That of Febrile Seizures

Frontiers in neurology, 2022-05, Vol.13, p.891721-891721

2022

Volltextzugriff (PDF)

Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data

Scientific reports, 2021-02, Vol.11 (1), p.3381-3381, Article 3381

2021

Volltextzugriff (PDF)

Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin

Brain & development (Tokyo. 1979), 2009-03, Vol.31 (3), p.221-227

2009

Volltextzugriff (PDF)

Identification of vaccine-derived rotavirus strains in children with acute gastroenteritis in Japan, 2012-2015

PloS one, 2017-09, Vol.12 (9), p.e0184067-e0184067

2017

Volltextzugriff (PDF)

Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases

Brain & development (Tokyo. 1979), 2011-06, Vol.33 (6), p.512-517

2011

Volltextzugriff (PDF)

Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex

Human genomics, 2023-02, Vol.17 (1), p.4-4, Article 4

2023

Volltextzugriff (PDF)

Molecular epidemiology and disease severity of human respiratory syncytial virus in Vietnam

PloS one, 2013-01, Vol.8 (1), p.e45436-e45436

2013

Volltextzugriff (PDF)

Clinical and genetic features of acute encephalopathy in children taking theophylline

Brain & development (Tokyo. 1979), 2015-05, Vol.37 (5), p.463-470

2015

Volltextzugriff (PDF)

Brain hyperserotonemia causes autism-relevant social deficits in mice

Molecular autism, 2018-11, Vol.9 (1), p.60-60, Article 60

2018

Volltextzugriff (PDF)

Association of human cytomegalovirus (HCMV) neutralizing antibodies with antibodies to the HCMV glycoprotein complexes

Virology journal, 2020-08, Vol.17 (1), p.1-120, Article 120

2020

Volltextzugriff (PDF)

Expression of insulin-like growth factors (IGFs) and IGF signaling: molecular complexity in uterine leiomyomas

Fertility and sterility, 2009-06, Vol.91 (6), p.2664-2675

2009

Volltextzugriff (PDF)

Case Report: Tuberous sclerosis complex-associated hemihypertrophy successfully treated with mTOR inhibitor sirolimus

Frontiers in pediatrics, 2024-02, Vol.12, p.1333064

2024

Volltextzugriff (PDF)

TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity

PloS one, 2013-01, Vol.8 (1), p.e54503

2013

Volltextzugriff (PDF)

Mutations of the SCN1A gene in acute encephalopathy

Epilepsia (Copenhagen), 2012-03, Vol.53 (3), p.558-564

2012

Volltextzugriff (PDF)

A case of recurrent encephalopathy with SCN2A missense mutation

Brain & development (Tokyo. 1979), 2015-06, Vol.37 (6), p.631-634

2015

Volltextzugriff (PDF)

Brain edema with clasmatodendrosis complicating ataxia telangiectasia

Brain & development (Tokyo. 1979), 2017-08, Vol.39 (7), p.629-632

2017

Volltextzugriff (PDF)

Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34

Brain & development (Tokyo. 1979), 2015-08, Vol.37 (7), p.714-718

2015

Volltextzugriff (PDF)

Immunomodulatory therapy in recurrent acute necrotizing encephalopathy ANE1: Is it useful?

Brain & development (Tokyo. 1979), 2012-05, Vol.34 (5), p.384-391

2012

Volltextzugriff (PDF)

Manifestations and characteristics of congenital adrenal hyperplasia-associated encephalopathy

Brain & development (Tokyo. 1979), 2016-08, Vol.38 (7), p.638-647

2016

Volltextzugriff (PDF)

Seasonal pattern and genotype distribution of norovirus infection in Japan

The Pediatric infectious disease journal, 2010-05, Vol.29 (5), p.e32-e34

2010

Volltextzugriff (PDF)

1 – 25 von 89

Suche als RSS-Feed

Aktive Filter

KollektionIngentaConnect Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(89)
Mit Volltextzugriff
(84)

Publikationsform

Artikel
(89)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(78)
Life Sciences & Biomedicine
(58)
Humans
(53)
Neurosciences & Neurology
(37)
Neurology
(32)
Clinical Neurology
(31)
Female
(31)
Male
(31)
Pediatrics
(30)
Infant
(23)
Child
(21)
Biological And Medical Sciences
(19)
Child, Preschool
(19)
Animals
(15)
Medical Sciences
(15)
Multidisciplinary Sciences
(15)
Science & Technology - Other Topics
(15)
Mice
(12)
Neurosciences
(10)
Adolescent
(8)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Brain Symptoms of Tuberous Sclerosis Complex: Pathogenesis and Treatment

Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes

Comprehensive behavioral analysis of the Cdkl5 knockout mice revealed significant enhancement in anxiety- and fear-related behaviors and impairment in both acquisition and long-term retention of spatial reference memory

GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion

A severity score for acute necrotizing encephalopathy

Association of IL-1B rs16944 Polymorphism With Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion Is Opposite to That of Febrile Seizures

Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data

Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin

Identification of vaccine-derived rotavirus strains in children with acute gastroenteritis in Japan, 2012-2015

Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases

Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex

Molecular epidemiology and disease severity of human respiratory syncytial virus in Vietnam

Clinical and genetic features of acute encephalopathy in children taking theophylline

Brain hyperserotonemia causes autism-relevant social deficits in mice

Association of human cytomegalovirus (HCMV) neutralizing antibodies with antibodies to the HCMV glycoprotein complexes

Expression of insulin-like growth factors (IGFs) and IGF signaling: molecular complexity in uterine leiomyomas

Case Report: Tuberous sclerosis complex-associated hemihypertrophy successfully treated with mTOR inhibitor sirolimus

TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity

Mutations of the SCN1A gene in acute encephalopathy

A case of recurrent encephalopathy with SCN2A missense mutation

Brain edema with clasmatodendrosis complicating ataxia telangiectasia

Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34

Immunomodulatory therapy in recurrent acute necrotizing encephalopathy ANE1: Is it useful?

Manifestations and characteristics of congenital adrenal hyperplasia-associated encephalopathy

Seasonal pattern and genotype distribution of norovirus infection in Japan

Aktive Filter

Suchergebnisse filtern