UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Neuropathology of genetically defined malformations of cortical development—A systematic literature review

Neuropathology and applied neurobiology, 2021-08, Vol.47 (5), p.585-602

2021

Link zum Volltext

Verfügbarkeit prüfen

Myelin Pathology Beyond White Matter in Tuberous Sclerosis Complex (TSC) Cortical Tubers

Journal of neuropathology and experimental neurology, 2020-10, Vol.79 (10), p.1054-1064

2020

Link zum Volltext

Verfügbarkeit prüfen

Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM

BMC medicine, 2023-08, Vol.21 (1), p.298-298, Article 298

2023

Link zum Volltext

Verfügbarkeit prüfen

Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline

Brain (London, England : 1878), 2016-09, Vol.139 (Pt 9), p.2420-2430

2016

Link zum Volltext

Verfügbarkeit prüfen

A step-wise approach for establishing a multidisciplinary team for the management of tuberous sclerosis complex: a Delphi consensus report

Orphanet journal of rare diseases, 2019-04, Vol.14 (1), p.91-91, Article 91

2019

Link zum Volltext

Verfügbarkeit prüfen

Correction: Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM

BMC medicine, 2023-10, Vol.21 (1), p.401-401, Article 401

2023

Link zum Volltext

Verfügbarkeit prüfen

The histopathology of polymicrogyria: a series of 71 brain autopsy studies

Developmental medicine and child neurology, 2016-01, Vol.58 (1), p.39-48

2016

Link zum Volltext

Verfügbarkeit prüfen

mTOR-related neuropathology in mutant tsc2 zebrafish: Phenotypic, transcriptomic and pharmacological analysis

Neurobiology of disease, 2017-12, Vol.108, p.225-237

2017

Link zum Volltext

Verfügbarkeit prüfen

Diagnostic work-up in malformations of cortical development

Developmental medicine and child neurology, 2024-02

2024

Link zum Volltext

Verfügbarkeit prüfen

Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly

Frontiers in genetics, 2020-02, Vol.11, p.26

2020

Link zum Volltext

Verfügbarkeit prüfen

The research landscape of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)-a comprehensive scoping review

Journal of neurodevelopmental disorders, 2022-02, Vol.14 (1), p.13-13, Article 13

2022

Link zum Volltext

Verfügbarkeit prüfen

International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)

Journal of neurodevelopmental disorders, 2023-09, Vol.15 (1), p.32-32, Article 32

2023

Link zum Volltext

Verfügbarkeit prüfen

Empowering Families Through Technology: A Mobile-Health Project to Reduce the TAND Identification and Treatment Gap (TANDem)

Frontiers in psychiatry, 2022-02, Vol.13, p.834628-834628

2022

Link zum Volltext

Verfügbarkeit prüfen

Care for the caregiver! A call for action

European journal of paediatric neurology, 2021-11, Vol.35, p.A3-A4

Jansen, Anna C.

2021

Link zum Volltext

Verfügbarkeit prüfen

Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?

Annals of clinical and translational neurology, 2020-08, Vol.7 (8), p.1371-1381

2020

Link zum Volltext

Verfügbarkeit prüfen

Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes

Hereditary cancer in clinical practice, 2018-01, Vol.16 (1), p.2-2, Article 2

2018

Link zum Volltext

Verfügbarkeit prüfen

Management of epilepsy associated with tuberous sclerosis complex: Updated clinical recommendations

European journal of paediatric neurology, 2018-09, Vol.22 (5), p.738-748

2018

Link zum Volltext

Verfügbarkeit prüfen

A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease

Hereditary cancer in clinical practice, 2019-07, Vol.17 (1), p.22-22, Article 22

2019

Link zum Volltext

Verfügbarkeit prüfen

Macrocephaly? Do not Forget SUFU

Pediatric neurology, 2024-02, Vol.151, p.34-36

2024

Link zum Volltext

Verfügbarkeit prüfen

Infants dying suddenly and unexpectedly share demographic features with infants who die with retinal and dural bleeding: a review of neural mechanisms

Developmental medicine and child neurology, 2016-12, Vol.58 (12), p.1223-1234

2016

Link zum Volltext

Verfügbarkeit prüfen

Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.1943-1953

2022

Link zum Volltext

Verfügbarkeit prüfen

Malformations of cerebral development and clues from the peripheral nervous system: A systematic literature review

European journal of paediatric neurology, 2022-03, Vol.37, p.155-164

2022

Link zum Volltext

Verfügbarkeit prüfen

TuberOus SClerosis registry to increase disease Awareness (TOSCA) - baseline data on 2093 patients

Orphanet journal of rare diseases, 2017-01, Vol.12 (1), p.2-2, Article 2

2017

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 339

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(322)
Mit Volltextzugriff
(308)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Neuropathology of genetically defined malformations of cortical development—A systematic literature review

Myelin Pathology Beyond White Matter in Tuberous Sclerosis Complex (TSC) Cortical Tubers

Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM

Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline

A step-wise approach for establishing a multidisciplinary team for the management of tuberous sclerosis complex: a Delphi consensus report

Prediction of Neurodevelopment in Infants With Tuberous Sclerosis Complex Using Early EEG Characteristics

Correction: Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM

The histopathology of polymicrogyria: a series of 71 brain autopsy studies

mTOR-related neuropathology in mutant tsc2 zebrafish: Phenotypic, transcriptomic and pharmacological analysis

Diagnostic work-up in malformations of cortical development

Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly

The research landscape of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)-a comprehensive scoping review

International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)

Empowering Families Through Technology: A Mobile-Health Project to Reduce the TAND Identification and Treatment Gap (TANDem)

Care for the caregiver! A call for action

Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?

Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes

miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis Complex

Management of epilepsy associated with tuberous sclerosis complex: Updated clinical recommendations

A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease

Macrocephaly? Do not Forget SUFU

Infants dying suddenly and unexpectedly share demographic features with infants who die with retinal and dural bleeding: a review of neural mechanisms

Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children

Malformations of cerebral development and clues from the peripheral nervous system: A systematic literature review

TuberOus SClerosis registry to increase disease Awareness (TOSCA) - baseline data on 2093 patients

Suchergebnisse filtern