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...

Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and Obstetricians

European Journal of Obstetrics & Gynecology and Reproductive Biology, 2015-10, Vol.193, p.10-18

2015

Volltextzugriff (PDF)

Rationale and design of the multicentric, double-blind, double-placebo, randomized trial APrepitant versus HYdroxyzine in association with cytoreductive treatments for patients with myeloproliferative neoplasia suffering from Persistent Aquagenic Pruritus. Trial acronym: APHYPAP

Trials, 2021-12, Vol.22 (1), p.938-938, Article 938

2021

Volltextzugriff (PDF)

Small‐fibre neuropathy and pruritus: histological patterns of nerve fibres in skin biopsies

British journal of dermatology (1951), 2020-02, Vol.182 (2), p.504-506

2020

Volltextzugriff (PDF)

Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series

Journal of neurology, neurosurgery and psychiatry, 2010, Vol.81 (1), p.101-104

2010

Volltextzugriff (PDF)

Overexpression of certain transient receptor potential and Orai channels in prostate cancer is associated with decreased risk of systemic recurrence after radical prostatectomy

The Prostate, 2019-12, Vol.79 (16), p.1793-1804

2019

Volltextzugriff (PDF)

Exercise testing‐based algorithms to diagnose McArdle disease and MAD defects

Acta neurologica Scandinavica, 2018-10, Vol.138 (4), p.301-307

2018

Volltextzugriff (PDF)

ALK FISH rearranged and amplified tumor with negative immunohistochemistry: a rare and challenging case concerning ALK status screening in lung cancer

Annals of oncology, 2015-07, Vol.26 (7), p.1514-1515

2015

Volltextzugriff (PDF)

Presence of putative stem cells in Merkel cell carcinomas

Journal of the European Academy of Dermatology and Venereology, 2012-06, Vol.26 (6), p.789-795

2012

Volltextzugriff (PDF)

Anti-HMG-CoA reductase necrotizing myopathy: A report of 4 cases

La revue de medecine interne, 2017-04, Vol.38 (4), p.228

2017

Volltextzugriff (PDF)

Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene

Neurology, 2010-02, Vol.74 (6), p.507

2010

Volltextzugriff (PDF)

OP0189 High Grade Salivary Gland Involvement, Assessed by Histology or Ultrasonography, Is Associated with a Poor Response to Rituximab in Primary Sjögren's Syndrome Patients

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.143-143

2015

Volltextzugriff (PDF)

SAT0382 B and T Cells Count in Minor Salivary Glands of Primary SjÖgren's Syndrome: Development and Validation of a Digital Procedure

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.797-798

2015

Volltextzugriff (PDF)

Small fiber neuropathy

La revue de medecine interne, 2018-02, Vol.39 (2), p.99-106

2018

Volltextzugriff (PDF)

Diagnosis of small-fibre neuropathies: comparison between quantitative sensory testing and the measurement of intraepidermal nerve fibre density

Journal of the European Academy of Dermatology and Venereology, 2014-06, Vol.28 (6), p.825-826

2014

Volltextzugriff (PDF)

Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis

Neuromuscular disorders : NMD, 2016-10, Vol.26 (suppl 2), p.S118-S119

2016

Volltextzugriff (PDF)

Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis

Molecular syndromology, 2013-09, Vol.4 (6), p.267-272

2013

Volltextzugriff (PDF)

Basal ganglia involvement in ARX gene mutated patients: The reason for very specific grasping in ARX mutated patients?

European journal of paediatric neurology, 2017-06, Vol.21, p.e62-e62

2017

Volltextzugriff (PDF)

Molecular heterogeneity in fetal forms of type II lissencephaly

Human mutation, 2007-10, Vol.28 (10), p.1020-1027

2007

Volltextzugriff (PDF)

SAT0217 Diagnostic value of labial minor salivary gland biopsy for primary sjögren’s syndrome: A systematic review

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.545-545

2013

Volltextzugriff (PDF)

Neuropathic pruritus

Nature reviews. Neurology, 2014-07, Vol.10 (7), p.408-416

2014

Volltextzugriff (PDF)

Placental features in intrauterine growth retardation

Journal de gynecologie, obstetrique et biologie de la reproduction, 2013-12, Vol.42 (8), p.996

Marcorelles, P

2013

Volltextzugriff (PDF)

Neuropathie à petites fibres : le point de vue du neuropathologiste. L’étude des fibres nerveuses intra-épidermiques

Pratique neurologique - FMC, 2022-06, Vol.13 (2), p.112-115

2022

Volltextzugriff (PDF)

Fatal congenital tuberculosis due to a Beijing strain in a premature neonate

Journal of medical microbiology, 2010-06, Vol.59 (6), p.733-735

2010

Volltextzugriff (PDF)

Défaut de maturation placentaire: une pathologie placentaire de diagnostic anatomopathologique

Revue de médecine périnatale, 2011-12, Vol.3 (4), p.185-188

2011

Volltextzugriff (PDF)

1 – 25 von 123

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

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

Publikationsform

Artikel
(122)
Berichte
(1)

Sprache

Englisch
(62)
Französisch
(62)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and Obstetricians

OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

Rationale and design of the multicentric, double-blind, double-placebo, randomized trial APrepitant versus HYdroxyzine in association with cytoreductive treatments for patients with myeloproliferative neoplasia suffering from Persistent Aquagenic Pruritus. Trial acronym: APHYPAP

Small‐fibre neuropathy and pruritus: histological patterns of nerve fibres in skin biopsies

Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series

Overexpression of certain transient receptor potential and Orai channels in prostate cancer is associated with decreased risk of systemic recurrence after radical prostatectomy

Exercise testing‐based algorithms to diagnose McArdle disease and MAD defects

ALK FISH rearranged and amplified tumor with negative immunohistochemistry: a rare and challenging case concerning ALK status screening in lung cancer

Presence of putative stem cells in Merkel cell carcinomas

Anti-HMG-CoA reductase necrotizing myopathy: A report of 4 cases

Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene

OP0189 High Grade Salivary Gland Involvement, Assessed by Histology or Ultrasonography, Is Associated with a Poor Response to Rituximab in Primary Sjögren's Syndrome Patients

SAT0382 B and T Cells Count in Minor Salivary Glands of Primary SjÖgren's Syndrome: Development and Validation of a Digital Procedure

Small fiber neuropathy

Diagnosis of small-fibre neuropathies: comparison between quantitative sensory testing and the measurement of intraepidermal nerve fibre density

Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis

Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis

Basal ganglia involvement in ARX gene mutated patients: The reason for very specific grasping in ARX mutated patients?

Molecular heterogeneity in fetal forms of type II lissencephaly

SAT0217 Diagnostic value of labial minor salivary gland biopsy for primary sjögren’s syndrome: A systematic review

Neuropathic pruritus

Placental features in intrauterine growth retardation

Neuropathie à petites fibres : le point de vue du neuropathologiste. L’étude des fibres nerveuses intra-épidermiques

Fatal congenital tuberculosis due to a Beijing strain in a premature neonate

Défaut de maturation placentaire: une pathologie placentaire de diagnostic anatomopathologique

Suchergebnisse filtern