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...

DWI Hyperintensity in the Fornix Fimbria on MRI in Children

American journal of neuroradiology : AJNR, 2022-03, Vol.43 (3), p.480-485

2022

Volltextzugriff (PDF)

PP01.8 – 2708: Lissencephaly with gray matter heterotopias and spinal dysraphism – A new syndrome

European journal of paediatric neurology, 2015-05, Vol.19, p.S31-S31

2015

Volltextzugriff (PDF)

The Globe and Orbit in Laron Syndrome

American journal of neuroradiology : AJNR, 2011-09, Vol.32 (8), p.1560-1562

2011

Volltextzugriff (PDF)

Optic Pathway Glioma: Correlation of Imaging Findings with the Presence of Neurofibromatosis

American journal of neuroradiology, 2001-11, Vol.22 (10), p.1963-1969

2001

Volltextzugriff (PDF)

A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family

European journal of paediatric neurology, 2013-05, Vol.17 (3), p.259-264

2013

Volltextzugriff (PDF)

Craniofacial and brain abnormalities in Laron syndrome (primary growth hormone insensitivity)

European journal of endocrinology, 2002-04, Vol.146 (4), p.499-503

2002

Volltextzugriff (PDF)

The Intellectual Capacity of Patients with Laron Syndrome (LS) Differs with Various Molecular Defects of the Growth Hormone Receptor Gene. Correlation with CNS Abnormalities

Hormone and metabolic research, 2005-12, Vol.37 (12), p.757-760

2005

Volltextzugriff (PDF)

A new mutation in the growth hormone-releasing hormone receptor gene in two Israeli Arab families

Journal of endocrinological investigation, 2006-02, Vol.29 (2), p.122-130

2006

Volltextzugriff (PDF)

Hand Size and Growth in Untreated and IGF-I Treated Patients with Laron Syndrome

Journal of Pediatric Endocrinology and Metabolism, 2009-03, Vol.22 (3), p.235-240

2009

Volltextzugriff (PDF)

Growth Hormone Replacement Therapy Seems to Be Safe in Children with Low-Grade Midline Glioma: A Series of 124 Cases with Review of the Literature

Cancers, 2022-12, Vol.15 (1), p.55

2022

Volltextzugriff (PDF)

B022 Cochlear implantation in the presence of inner ear anomalies: surgical and functional outcomes

International journal of pediatric otorhinolaryngology, 2011, Vol.75, p.14-14

2011

Volltextzugriff (PDF)

Abnormalities of the axial and proximal appendicular skeleton in adults with Laron syndrome (growth hormone insensitivity)

Skeletal radiology, 2008-02, Vol.37 (2), p.153-160

2008

Volltextzugriff (PDF)

Familial infantile bilateral striatal necrosis: clinical features and response to biotin treatment

Neurology, 2002-10, Vol.59 (7), p.983-989

2002

Volltextzugriff (PDF)

Sibling influence, gender roles, and the sexual socialization of urban early adolescent girls

The Journal of sex research, 2003-02, Vol.40 (1), p.101-110

2003

Volltextzugriff (PDF)

Melanoma cell lines from different stages of progression and their biological and molecular analyses

Melanoma research, 1997-08, Vol.7 Suppl 2 (SUPPLEMENT 2), p.S35

1997

Volltextzugriff (PDF)

PROP-1 gene mutation (R120C) causing combined pituitary hormone deficiencies with variable clinical course in eight siblings of one Jewish Moroccan family

Hormone research, 2003-01, Vol.60 (5), p.227-231

2003

Volltextzugriff (PDF)

Hepatic iron overload: quantitative MR imaging

Radiology, 1991-05, Vol.179 (2), p.367-369

1991

Volltextzugriff (PDF)

Familial hemophagocytic lymphohistiocytosis: Improved neurodevelopmental outcome after bone marrow transplantation

The Journal of pediatrics, 1998-07, Vol.133 (1), p.126-128

1998

Volltextzugriff (PDF)

MRI in acute poliomyelitis

Neuroradiology, 1996-05, Vol.38 (4), p.371-372

1996

Volltextzugriff (PDF)

Metastatic brain involvement in Ewing family of tumors in children

Neurology, 1998-11, Vol.51 (5), p.1336-1338

1998

Volltextzugriff (PDF)

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

European journal of haematology, 2005-02, Vol.74 (2), p.93-100

2005

Volltextzugriff (PDF)

Visual pathway glioma: an erratic tumour with therapeutic dilemmas

Archives of disease in childhood, 1997-03, Vol.76 (3), p.259-263

1997

Volltextzugriff (PDF)

Clinical and sonographic criteria of acute scrotum in children: a retrospective study of 172 boys

Pediatric radiology, 2005-03, Vol.35 (3), p.302-310

2005

Volltextzugriff (PDF)

Iron overload following bone marrow transplantation in children : MR findings

Pediatric radiology, 1997-11, Vol.27 (11), p.869-872

1997

Volltextzugriff (PDF)

Tietze’s syndrome in children and infants

The Journal of pediatrics, 1997-11, Vol.131 (5), p.774-775

1997

Volltextzugriff (PDF)

1 – 25 von 271

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(225)
Mit Volltextzugriff
(196)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(161)
Science & Technology
(156)
Life Sciences & Biomedicine
(142)
Male
(99)
Female
(88)
Biological And Medical Sciences
(84)
Medical Sciences
(81)
Child
(64)
Child, Preschool
(49)
Adult
(48)
Pediatrics
(47)
Adolescent
(38)
Radiology, Nuclear Medicine & Medical Imaging
(36)
Infant
(35)
Magnetic Resonance Imaging
(30)
Neurosciences & Neurology
(30)
Middle Aged
(27)
Clinical Neurology
(26)
Neurology
(22)
Tomography, X-Ray Computed
(21)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

DWI Hyperintensity in the Fornix Fimbria on MRI in Children

PP01.8 – 2708: Lissencephaly with gray matter heterotopias and spinal dysraphism – A new syndrome

The Globe and Orbit in Laron Syndrome

Optic Pathway Glioma: Correlation of Imaging Findings with the Presence of Neurofibromatosis

A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family

Craniofacial and brain abnormalities in Laron syndrome (primary growth hormone insensitivity)

The Intellectual Capacity of Patients with Laron Syndrome (LS) Differs with Various Molecular Defects of the Growth Hormone Receptor Gene. Correlation with CNS Abnormalities

A new mutation in the growth hormone-releasing hormone receptor gene in two Israeli Arab families

Hand Size and Growth in Untreated and IGF-I Treated Patients with Laron Syndrome

Growth Hormone Replacement Therapy Seems to Be Safe in Children with Low-Grade Midline Glioma: A Series of 124 Cases with Review of the Literature

B022 Cochlear implantation in the presence of inner ear anomalies: surgical and functional outcomes

Abnormalities of the axial and proximal appendicular skeleton in adults with Laron syndrome (growth hormone insensitivity)

Familial infantile bilateral striatal necrosis: clinical features and response to biotin treatment

Sibling influence, gender roles, and the sexual socialization of urban early adolescent girls

Melanoma cell lines from different stages of progression and their biological and molecular analyses

PROP-1 gene mutation (R120C) causing combined pituitary hormone deficiencies with variable clinical course in eight siblings of one Jewish Moroccan family

Hepatic iron overload: quantitative MR imaging

Familial hemophagocytic lymphohistiocytosis: Improved neurodevelopmental outcome after bone marrow transplantation

MRI in acute poliomyelitis

Metastatic brain involvement in Ewing family of tumors in children

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

Visual pathway glioma: an erratic tumour with therapeutic dilemmas

Clinical and sonographic criteria of acute scrotum in children: a retrospective study of 172 boys

Iron overload following bone marrow transplantation in children : MR findings

Tietze’s syndrome in children and infants

Suchergebnisse filtern