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...

Conceiving a hematopoietic stem cell donor: twenty-five years after our decision to save a child

Haematologica (Roma), 2012-04, Vol.97 (4), p.479-481

2012

Volltextzugriff (PDF)

Reply to "Ethical concerns surrounding the conception of an HLA-compatible child for medical purposes" Haematologica 2012;97(9):e33

Haematologica (Roma), 2012-09, Vol.97 (9), p.e36-e36

2012

Volltextzugriff (PDF)

Drug resistant epilepsy in a young male with Cat Eye Syndrome: a case study

Clinical Cases and Reviews in Epilepsy, 2017, Vol.2 (1-4), p.15

Verri, Annapia

2017

Volltextzugriff (PDF)

Late onset myoclonic epilepsy in Down syndrome and dementia

Clinical management issues, 2012-09, Vol.6 (3), p.97-103

2012

Volltextzugriff (PDF)

A Precocious Cerebellar Ataxia and Frequent Fever Episodes in a 16-Month-Old Infant Revealing Ataxia-Telangiectasia Syndrome

Case reports in immunology, 2013-01, Vol.2013 (2013), p.1-5

2013

Volltextzugriff (PDF)

Psychotic disorder and its characteristics in sex chromosome aneuploidies

Clinical management issues, 2009-09, Vol.3 (3), p.123-132

2009

Volltextzugriff (PDF)

Variability in genetic syndromes: Some lessons from history

Journal of intellectual disability research, 2010-10, Vol.54 (10), p.877-880

2010

Volltextzugriff (PDF)

Klinefelter's syndrome and psychoneurologic function

Molecular human reproduction, 2010-06, Vol.16 (6), p.425-433

2010

Volltextzugriff (PDF)

Early/late-life adversities and behavioural phenotypes: insight into metabolomics, genomics and connectomics

Journal of intellectual disability research, 2016-09, Vol.60 (9), p.833-834

2016

Volltextzugriff (PDF)

Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature

Molecular cytogenetics, 2016-02, Vol.9 (1), p.21-21, Article 21

2016

Volltextzugriff (PDF)

Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature

European journal of medical genetics, 2018-03, Vol.61 (3), p.173-180

2018

Volltextzugriff (PDF)

Relevance of clinical context in the diagnostic‐therapeutic approach to status epilepticus

Epilepsia (Copenhagen), 2016-09, Vol.57 (9), p.1527-1529

2016

Volltextzugriff (PDF)

Molecular and clinical characterization of patients with overlapping 10p deletions

American journal of medical genetics. Part A, 2010-05, Vol.152A (5), p.1233-1243

2010

Volltextzugriff (PDF)

Variability in Cognitive Behavioral Phenotypes in Klinefelter Syndrome (KS) and Other Sex Chromosomal Aneuploidies (SCAs)

Journal of Antimicrobial Agents, 2017, Vol.6 (1)

2017

Volltextzugriff (PDF)

Klinefelter's syndrome and psychoneurologic function : Klinefelter's syndrome: basic science to clinic

Molecular human reproduction, 2010, Vol.16 (5-6), p.425-433

2010

Volltextzugriff (PDF)

Referential Choice in the Narratives of Italian Speakers with Klinefelter Syndrome

International journal of speech & language pathology and audiology, 2014-09, Vol.2 (2), p.81-85

2014

Volltextzugriff (PDF)

Body dissatisfaction, disordered eating, fashion magazines, and clothes: A cross-cultural comparison between Australian and Italian young women

International journal of psychology, 2005-10, Vol.40 (5), p.293-302

2005

Volltextzugriff (PDF)

Interferon-γ- and interleukin-4-producing T cells in Down's syndrome

Neuroscience letters, 2006-02, Vol.395 (1), p.67-70

2006

Volltextzugriff (PDF)

Psychiatric comorbidity in chronic daily headache

Cephalalgia, 1998, Vol.18

Verri, Annapia

1998

Volltextzugriff (PDF)

Premenstrual dysphoric disorder and eating disorders

Cephalalgia, 1997, Vol.17

Verri, Annapia

1997

Volltextzugriff (PDF)

Food-related problems in Klinefelter Syndrome? A probable case of Pica

Minerva pediatrica, 2020-04, Vol.72 (2)

2020

Volltextzugriff (PDF)

Late diagnosis in severe and mild intellectual disability in adulthood

Journal of intellectual disability research, 2004-10, Vol.48 (7), p.679-686

2004

Volltextzugriff (PDF)

Oral self-mutilation in a patient with rhombencephalosynapsys

Journal of intellectual disability research, 2000-02, Vol.44 (1), p.86-90

2000

Volltextzugriff (PDF)

Contingent negative variation indicates phasic arousal for externally cued unilateral eye blink in human subjects

Neuroscience letters, 1999-04, Vol.266 (1), p.57-60

1999

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(26)

Publikationsform

Artikel
(30)

Sprache

Englisch
(30)
Italienisch
(2)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(21)
Science & Technology
(21)
Humans
(13)
Biological And Medical Sciences
(9)
Male
(9)
Neurosciences & Neurology
(9)
Adult
(8)
Genetics & Heredity
(8)
Clinical Neurology
(7)
Female
(7)
Medical Sciences
(7)
Psychiatry
(6)
Social Sciences
(6)
Fundamental And Applied Biological Sciences. Psychology
(5)
Chromosome Aberrations
(4)
Education & Educational Research
(4)
Education, Special
(4)
Mental Retardation
(4)
Pregnancy
(4)
Psychology. Psychoanalysis. Psychiatry
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Conceiving a hematopoietic stem cell donor: twenty-five years after our decision to save a child

Reply to "Ethical concerns surrounding the conception of an HLA-compatible child for medical purposes" Haematologica 2012;97(9):e33

Drug resistant epilepsy in a young male with Cat Eye Syndrome: a case study

Late onset myoclonic epilepsy in Down syndrome and dementia

A Precocious Cerebellar Ataxia and Frequent Fever Episodes in a 16-Month-Old Infant Revealing Ataxia-Telangiectasia Syndrome

Psychotic disorder and its characteristics in sex chromosome aneuploidies

Variability in genetic syndromes: Some lessons from history

Klinefelter's syndrome and psychoneurologic function

Antidepressant effect of vagal nerve stimulation in epilepsy patients: a systematic review

Early/late-life adversities and behavioural phenotypes: insight into metabolomics, genomics and connectomics

Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature

Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature

Relevance of clinical context in the diagnostic‐therapeutic approach to status epilepticus

Molecular and clinical characterization of patients with overlapping 10p deletions

Variability in Cognitive Behavioral Phenotypes in Klinefelter Syndrome (KS) and Other Sex Chromosomal Aneuploidies (SCAs)

Klinefelter's syndrome and psychoneurologic function : Klinefelter's syndrome: basic science to clinic

Referential Choice in the Narratives of Italian Speakers with Klinefelter Syndrome

Body dissatisfaction, disordered eating, fashion magazines, and clothes: A cross-cultural comparison between Australian and Italian young women

Interferon-γ- and interleukin-4-producing T cells in Down's syndrome

Psychiatric comorbidity in chronic daily headache

Premenstrual dysphoric disorder and eating disorders

Food-related problems in Klinefelter Syndrome? A probable case of Pica

Late diagnosis in severe and mild intellectual disability in adulthood

Oral self-mutilation in a patient with rhombencephalosynapsys

Contingent negative variation indicates phasic arousal for externally cued unilateral eye blink in human subjects

Suchergebnisse filtern