UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 114

Sortiert nach

Congenital malformation of dural sinus that resolved spontaneously

Anales de Pediatría, 2020-04, Vol.92 (4), p.245-246

2020

Volltextzugriff (PDF)

A novel de novo MTOR gain-of-function variant in a patient with Smith-Kingsmore syndrome and Antiphospholipid syndrome

European journal of human genetics : EJHG, 2019-09, Vol.27 (9), p.1369-1378

2019

Volltextzugriff (PDF)

Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review

Brain & development (Tokyo. 1979), 2018-04, Vol.40 (4), p.348-352

2018

Volltextzugriff (PDF)

Differential dorsolateral prefrontal cortex activation during a verbal n-back task according to sensory modality

Behavioural brain research, 2009-12, Vol.205 (1), p.299-302

2009

Volltextzugriff (PDF)

Posterior reversible encephalopathy syndrome (PRES): a rare condition after resection of posterior fossa tumors: two new cases and review of the literature

Child's nervous system, 2016-05, Vol.32 (5), p.857-863

2016

Volltextzugriff (PDF)

Failure of deactivation in bipolar disorder during performance of an fMRI adapted version of the Stroop task

Journal of affective disorders, 2023-05, Vol.329, p.307-314

2023

Volltextzugriff (PDF)

Activation and deactivation patterns in schizophrenia during performance of an fMRI adapted version of the stroop task

Journal of psychiatric research, 2021-12, Vol.144, p.1-7

2021

Volltextzugriff (PDF)

Effects of perinatal HIV-infection on the cortical thickness and subcortical gray matter volumes in young adulthood

Medicine (Baltimore), 2021-04, Vol.100 (15), p.e25403-e25403

2021

Volltextzugriff (PDF)

A novel de novo variant in CASK causes a severe neurodevelopmental disorder that masks the phenotype of a novel de novo variant in EEF2

Journal of human genetics, 2023-08, Vol.68 (8), p.543-550

2023

Volltextzugriff (PDF)

MAST1 variant causes mega‐corpus‐callosum syndrome with cortical malformations but without cerebellar hypoplasia

American journal of medical genetics. Part A, 2020-06, Vol.182 (6), p.1483-1490

2020

Volltextzugriff (PDF)

A Systematic Review of Magnetic Resonance Imaging Studies in Perinatally HIV-Infected Individuals

AIDS reviews, 2021-10, Vol.23 (4), p.167-185

2021

Volltextzugriff (PDF)

A novel de novo mutation in the PURA gene associated with a new clinical finding: large brainstem

Journal of genetics, 2020-12, Vol.99 (1), Article 7

2020

Volltextzugriff (PDF)

LAMA2-related congenital muscular dystrophy complicated by West syndrome

European journal of paediatric neurology, 2015-03, Vol.19 (2), p.243-247

2015

Volltextzugriff (PDF)

First missense mutation outside of SERAC1 lipase domain affecting intracellular cholesterol trafficking

Neurogenetics, 2016, Vol.17 (1), p.51-56

2016

Volltextzugriff (PDF)

First splicing variant in HECW2 with an autosomal recessive pattern of inheritance and associated with NDHSAL

Human mutation, 2022-10, Vol.43 (10), p.1361-1367

2022

Volltextzugriff (PDF)

Spontaneous carotid and vertebral artery dissection in children

Pediatric neurology, 2001-09, Vol.25 (3), p.250-253

2001

Volltextzugriff (PDF)

Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA1A Mutation

Headache, 2011-11, Vol.51 (10), p.1542-1546

2011

Volltextzugriff (PDF)

Stroke in paediatric patients with sickle-cell anaemia

Revista de neurologiá, 2014-08, Vol.59 (4), p.153-157

2014

Volltextzugriff (PDF)

Malformación congénita de seno dural con resolución espontánea

Anales de pediatría (Barcelona, Spain : 2003), 2020-04, Vol.92 (4), p.245-246

2020

Volltextzugriff (PDF)

Actividad cerebral en jóvenes infectados por el virus de la inmunodeficiencia humana por transmisión vertical: estudio piloto de resonancia magnética funcional

Revista de neurologiá, 2021-05, Vol.72 (10), p.343

2021

Volltextzugriff (PDF)

Steroids for familial acute necrotizing encephalopathy: A future investment?

Clinical neurology and neurosurgery, 2018-11, Vol.174, p.134-136

2018

Volltextzugriff (PDF)

Alteraciones del lenguaje en la cerebelitis aguda: más allá de la disartria

Revista de neurologiá, 2017, Vol.64 (1), p.27

2017

Volltextzugriff (PDF)

Distal phalangeal erythema in an infant with biallelic PDSS1 mutations: Expanding the phenotype of primary Coenzyme Q10 deficiency

JIMD reports, 2021-11, Vol.62 (1), p.3-5

2021

Volltextzugriff (PDF)

Longitudinal myelitis as the presenting symptom of neurosarcoidosis

Revista de neurologiá, 2010-09, Vol.51 (5), p.302-302

2010

Volltextzugriff (PDF)

Neurocutaneous Melanosis: An Illustrative Patient

Pediatric neurology, 2014-09, Vol.51 (3), p.468-469

2014

Volltextzugriff (PDF)

1 – 25 von 114

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(95)
Mit Volltextzugriff
(98)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

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

Menü

Weitere Dienste

Einstellungen

Congenital malformation of dural sinus that resolved spontaneously

A novel de novo MTOR gain-of-function variant in a patient with Smith-Kingsmore syndrome and Antiphospholipid syndrome

Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review

Differential dorsolateral prefrontal cortex activation during a verbal n-back task according to sensory modality

Posterior reversible encephalopathy syndrome (PRES): a rare condition after resection of posterior fossa tumors: two new cases and review of the literature

Failure of deactivation in bipolar disorder during performance of an fMRI adapted version of the Stroop task

Activation and deactivation patterns in schizophrenia during performance of an fMRI adapted version of the stroop task

Effects of perinatal HIV-infection on the cortical thickness and subcortical gray matter volumes in young adulthood

A novel de novo variant in CASK causes a severe neurodevelopmental disorder that masks the phenotype of a novel de novo variant in EEF2

MAST1 variant causes mega‐corpus‐callosum syndrome with cortical malformations but without cerebellar hypoplasia

A Systematic Review of Magnetic Resonance Imaging Studies in Perinatally HIV-Infected Individuals

A novel de novo mutation in the PURA gene associated with a new clinical finding: large brainstem

LAMA2-related congenital muscular dystrophy complicated by West syndrome

First missense mutation outside of SERAC1 lipase domain affecting intracellular cholesterol trafficking

First splicing variant in HECW2 with an autosomal recessive pattern of inheritance and associated with NDHSAL

Spontaneous carotid and vertebral artery dissection in children

Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA1A Mutation

Stroke in paediatric patients with sickle-cell anaemia

Malformación congénita de seno dural con resolución espontánea

Actividad cerebral en jóvenes infectados por el virus de la inmunodeficiencia humana por transmisión vertical: estudio piloto de resonancia magnética funcional

Steroids for familial acute necrotizing encephalopathy: A future investment?

Alteraciones del lenguaje en la cerebelitis aguda: más allá de la disartria

Distal phalangeal erythema in an infant with biallelic PDSS1 mutations: Expanding the phenotype of primary Coenzyme Q10 deficiency

Longitudinal myelitis as the presenting symptom of neurosarcoidosis

Neurocutaneous Melanosis: An Illustrative Patient

Suchergebnisse filtern