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...

GnRH receptor mutations in isolated gonadotropic deficiency

Molecular and cellular endocrinology, 2011-10, Vol.346 (1), p.21-28

2011

Volltextzugriff (PDF)

Diffusion‐weighted magnetic resonance imaging of the fetal brain in intrauterine growth restriction

Ultrasound in obstetrics & gynecology, 2017-07, Vol.50 (1), p.79-87

2017

Volltextzugriff (PDF)

SARS‐CoV‐2 infection as cause of in‐utero fetal death: regional multicenter cohort study

Ultrasound in obstetrics & gynecology, 2023-12, Vol.62 (6), p.867-874

2023

Volltextzugriff (PDF)

VP23.02: Congenital Tonate infection and associated ultrasound findings

Ultrasound in obstetrics & gynecology, 2020-10, Vol.56 (S1), p.155-155

2020

Volltextzugriff (PDF)

Fetal urine biochemistry at 13–23 weeks of gestation in lower urinary tract obstruction: criteria for in‐utero treatment

Ultrasound in obstetrics & gynecology, 2015-09, Vol.46 (3), p.306-311

2015

Volltextzugriff (PDF)

EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder

Clinical genetics, 2018-06, Vol.93 (6), p.1141-1147

2018

Volltextzugriff (PDF)

Sequential fetal serum β2‐microglobulin to predict postnatal renal function in bilateral or low urinary tract obstruction

Ultrasound in obstetrics & gynecology, 2017-05, Vol.49 (5), p.617-622

2017

Volltextzugriff (PDF)

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations

Neurology, 2009-09, Vol.73 (12), p.962-969

2009

Volltextzugriff (PDF)

Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome

Ultrasound in obstetrics & gynecology, 2013-03, Vol.41 (3), p.341-342

2013

Volltextzugriff (PDF)

Contribution of Diffusion-Weighted Imaging in the Evaluation of Diffuse White Matter Ischemic Lesions in Fetuses: Correlations with Fetopathologic Findings

American journal of neuroradiology : AJNR, 2008-01, Vol.29 (1), p.110-115

2008

Volltextzugriff (PDF)

L’analyse du transcriptome hypophysaire à 20 semaines de développement suggère un rôle important de ZEB2 dans le dimorphisme sexuel de la synthèse de la LH et de la FSH

Annales d'endocrinologie, 2015-09, Vol.76 (4), p.333-333

2015

Volltextzugriff (PDF)

Fetal obstructive uropathy complicated by urinary ascites: outcome and prognostic value of fetal serum [beta]-2-microglobulin

Ultrasound in obstetrics & gynecology, 2013-02, Vol.41 (2), p.185-189

2013

Volltextzugriff (PDF)

Fetal obstructive uropathy complicated by urinary ascites: outcome and prognostic value of fetal serum β‐2‐microglobulin

Ultrasound in obstetrics & gynecology, 2013-02, Vol.41 (2), p.185-189

2013

Volltextzugriff (PDF)

Les mouvements en miroir fréquemment observés chez les patients atteints d’un syndrome de Kallman par mutation d’ANOS1 (KAL1) sont dus à une anomalie de la décussation des faisceaux pyramidaux

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.255-256

2016

Volltextzugriff (PDF)

Molecular heterogeneity in fetal forms of type II lissencephaly

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

2007

Volltextzugriff (PDF)

3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome

Clinical genetics, 2012-08, Vol.82 (2), p.187-192

2012

Volltextzugriff (PDF)

Ultrasound detection of hyaloid artery in the third trimester of pregnancy: a pathological finding

Ultrasound in obstetrics & gynecology, 2012-04, Vol.39 (4), p.478-479

2012

Volltextzugriff (PDF)

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

American journal of medical genetics. Part A, 2013-01, Vol.161 (1), p.208-213

2013

Volltextzugriff (PDF)

Comparison between magnetic resonance imaging and fetopathology in the evaluation of fetal posterior fossa non‐cystic abnormalities

Ultrasound in obstetrics & gynecology, 2007-06, Vol.29 (6), p.651-659

2007

Volltextzugriff (PDF)

Very Early Twin-to-Twin Transfusion Syndrome and Discordant Activation of the Renin–Angiotensin System

Placenta (Eastbourne), 2009-08, Vol.30 (8), p.731-734

2009

Volltextzugriff (PDF)

Fetal neuroaxonal dystrophy: a further etiology of fetal akinesia

Canadian journal of neurological sciences, 2021-05, Vol.48 (s1), p.S4-S4

2021

Volltextzugriff (PDF)

La régulation négative de la concentration sérique de la LH et de la FSH du fœtus est associée à une perte de l’expression des Kisspeptines et de KISS1R dans l’hypothalamus tubéral en fin de développement

Annales d'endocrinologie, 2012-09, Vol.73 (4), p.250-250

2012

Volltextzugriff (PDF)

Contrôle hormonal de l’axe gonadotrope fœtal : un mécanisme complexe qui fait intervenir plusieurs boucles de régulation

Annales d'endocrinologie, 2023-10, Vol.84 (5), p.512-513

2023

Volltextzugriff (PDF)

Fetal neuroaxonal dystrophy: a new etiology of fetal akinesia

Canadian journal of neurological sciences, 2018-05, Vol.45 (S1), p.S3-S4

2018

Volltextzugriff (PDF)

1 – 25 von 49

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(46)
Mit Volltextzugriff
(47)

Publikationsform

Artikel
(46)
Berichte
(3)

Sprache

Englisch
(41)
Französisch
(8)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(27)
Science & Technology
(27)
Humans
(22)
Female
(17)
Pregnancy
(14)
Biological And Medical Sciences
(11)
Animals
(10)
Genetics & Heredity
(10)
Mice
(9)
Obstetrics & Gynecology
(9)
Medical Sciences
(8)
Radiology, Nuclear Medicine & Medical Imaging
(8)
Acoustics
(7)
Mutation
(7)
Prenatal Diagnosis
(7)
Technology
(7)
Adult
(6)
Fetuses
(6)
Gestational Age
(6)
Life Sciences
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

GnRH receptor mutations in isolated gonadotropic deficiency

Diffusion‐weighted magnetic resonance imaging of the fetal brain in intrauterine growth restriction

SARS‐CoV‐2 infection as cause of in‐utero fetal death: regional multicenter cohort study

VP23.02: Congenital Tonate infection and associated ultrasound findings

Fetal urine biochemistry at 13–23 weeks of gestation in lower urinary tract obstruction: criteria for in‐utero treatment

EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder

Sequential fetal serum β2‐microglobulin to predict postnatal renal function in bilateral or low urinary tract obstruction

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations

Ultrasound detection of eyelashes: a clue for prenatal diagnosis of Cornelia de Lange syndrome

Contribution of Diffusion-Weighted Imaging in the Evaluation of Diffuse White Matter Ischemic Lesions in Fetuses: Correlations with Fetopathologic Findings

L’analyse du transcriptome hypophysaire à 20 semaines de développement suggère un rôle important de ZEB2 dans le dimorphisme sexuel de la synthèse de la LH et de la FSH

Fetal obstructive uropathy complicated by urinary ascites: outcome and prognostic value of fetal serum [beta]-2-microglobulin

Fetal obstructive uropathy complicated by urinary ascites: outcome and prognostic value of fetal serum β‐2‐microglobulin

Les mouvements en miroir fréquemment observés chez les patients atteints d’un syndrome de Kallman par mutation d’ANOS1 (KAL1) sont dus à une anomalie de la décussation des faisceaux pyramidaux

Molecular heterogeneity in fetal forms of type II lissencephaly

3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome

Ultrasound detection of hyaloid artery in the third trimester of pregnancy: a pathological finding

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

Comparison between magnetic resonance imaging and fetopathology in the evaluation of fetal posterior fossa non‐cystic abnormalities

Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans

Very Early Twin-to-Twin Transfusion Syndrome and Discordant Activation of the Renin–Angiotensin System

Fetal neuroaxonal dystrophy: a further etiology of fetal akinesia

La régulation négative de la concentration sérique de la LH et de la FSH du fœtus est associée à une perte de l’expression des Kisspeptines et de KISS1R dans l’hypothalamus tubéral en fin de développement

Contrôle hormonal de l’axe gonadotrope fœtal : un mécanisme complexe qui fait intervenir plusieurs boucles de régulation

Fetal neuroaxonal dystrophy: a new etiology of fetal akinesia

Suchergebnisse filtern