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...

Hyperandrogenism in girls with juvenile neuronal ceroid lipofuscinosis

European journal of paediatric neurology, 2002, Vol.6 (4), p.199-205

2002

Volltextzugriff (PDF)

Oral dihydroergotamine for therapy-resistant migraine attacks in children

Pediatric neurology, 1997-02, Vol.16 (2), p.114-117

1997

Volltextzugriff (PDF)

New antidepressive and antipsychotic drugs in juvenile neuronal ceroid lipofuscinoses — a pilot study

European journal of paediatric neurology, 2001, Vol.5, p.163-166

2001

Volltextzugriff (PDF)

Rapid and simple assay for the determination of tripeptidyl peptidase and palmitoyl protein thioesterase activities in dried blood spots

Clinical chemistry (Baltimore, Md.), 2003-03, Vol.49 (3), p.509-511

2003

Volltextzugriff (PDF)

Clinical and magnetic resonance imaging findings in batten disease: Analysis of the major mutation (1.02-kb deletion)

Annals of neurology, 1997-11, Vol.42 (5), p.799-802

1997

Volltextzugriff (PDF)

Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses

American journal of human genetics, 1994-10, Vol.55 (4), p.695-701

1994

Volltextzugriff (PDF)

MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type

Neuroradiology, 1997-05, Vol.39 (5), p.371-377

1997

Volltextzugriff (PDF)

West syndrome: individualized ACTH therapy

Brain & development (Tokyo. 1979), 1996-11, Vol.18 (6), p.456-460

1996

Volltextzugriff (PDF)

MRI Evaluation of the Brain in Infantile Neuronal Ceroid-Lipofuscinosis: Part 2: MRI Findings in 21 Patients

Journal of child neurology, 1995-11, Vol.10 (6), p.444-450

1995

Volltextzugriff (PDF)

Bone-marrow transplantation in aspartylglucosaminuria

The Lancet (British edition), 1997-05, Vol.349 (9062), p.1366-1367

1997

Volltextzugriff (PDF)

Magnetic resonance techniques in neuronal ceroid lipofuscinoses and some other lysosomal diseases affecting the brain

Current opinion in neurology, 1997-12, Vol.10 (6), p.519

1997

Volltextzugriff (PDF)

Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1

Genomics (San Diego, Calif.), 1991, Vol.9 (1), p.170-173

1991

Volltextzugriff (PDF)

Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?

Annals of neurology, 1999-06, Vol.45 (6), p.801-805

1999

Volltextzugriff (PDF)

Batten disease gene, CLN3 : linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes

American journal of human genetics, 1995-03, Vol.56 (3), p.654-662

1995

Volltextzugriff (PDF)

Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI study

Neuropediatrics, 1999-12, Vol.30 (6), p.283-288

1999

Volltextzugriff (PDF)

Aspartylglucosaminuria: Radiologic Course of the Disease With Histopathologic Correlation

Journal of child neurology, 1997-09, Vol.12 (6), p.369-375

1997

Volltextzugriff (PDF)

Somatosensory Evoked Magnetic Fields From Primary Sensorimotor Cortex in Juvenile Neuronal Ceroid Lipofuscinosis

Journal of child neurology, 1997-09, Vol.12 (6), p.355-360

1997

Volltextzugriff (PDF)

Jansky-Bielschowsky variant disease: CT, MRI, and SPECT findings

Pediatric neurology, 1992-03, Vol.8 (2), p.121-126

1992

Volltextzugriff (PDF)

MRI Evaluation of the Brain in Infantile Neuronal Ceroid-Lipofuscinosis. Part 1: Postmortem MRI With Histopathologic Correlation

Journal of child neurology, 1995-11, Vol.10 (6), p.438-443

1995

Volltextzugriff (PDF)

Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi

Prenatal diagnosis, 1990-09, Vol.10 (9), p.553-559

1990

Volltextzugriff (PDF)

MRI Of the Brain, EEG Sleep Spindles and SPECT in the Early Diagnosis of Infantile Neuronal Ceroid Lipofuscinosis

Developmental medicine and child neurology, 1992-01, Vol.34 (1), p.61-65

1992

Volltextzugriff (PDF)

DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1)

Prenatal diagnosis, 1991-05, Vol.11 (5), p.323-328

1991

Volltextzugriff (PDF)

Strategy for mutation detection in CLN3: characterisation of two Finnish mutations

Neuropediatrics, 1997-02, Vol.28 (1), p.15-17

1997

Volltextzugriff (PDF)

Antioxidant treatment in Spielmeyer-Sjögren's disease

Acta neurologica Scandinavica, 1985-02, Vol.71 (2), p.136-145

1985

Volltextzugriff (PDF)

Can barbiturate anaesthesia cure infantile spasms?

Brain & development (Tokyo. 1979), 1988, Vol.10 (5), p.300-304

1988

Volltextzugriff (PDF)

1 – 25 von 25

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(20)

Publikationsform

Artikel
(25)

Sprache

Englisch
(25)

Erscheinungsjahr

n.n

Thema

Humans
(25)
Life Sciences & Biomedicine
(18)
Science & Technology
(18)
Biological And Medical Sciences
(16)
Female
(16)
Medical Sciences
(16)
Child
(15)
Male
(14)
Clinical Neurology
(12)
Magnetic Resonance Imaging
(12)
Neurosciences & Neurology
(12)
Child, Preschool
(9)
Medicin
(9)
Medicine
(9)
Metabolic Diseases
(9)
Neuronal Ceroid-Lipofuscinoses - Diagnosis
(9)
Pediatrics
(9)
Adolescent
(8)
Adult
(8)
Errors Of Metabolism
(8)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Hyperandrogenism in girls with juvenile neuronal ceroid lipofuscinosis

Oral dihydroergotamine for therapy-resistant migraine attacks in children

New antidepressive and antipsychotic drugs in juvenile neuronal ceroid lipofuscinoses — a pilot study

Rapid and simple assay for the determination of tripeptidyl peptidase and palmitoyl protein thioesterase activities in dried blood spots

Clinical and magnetic resonance imaging findings in batten disease: Analysis of the major mutation (1.02-kb deletion)

Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses

MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type

West syndrome: individualized ACTH therapy

MRI Evaluation of the Brain in Infantile Neuronal Ceroid-Lipofuscinosis: Part 2: MRI Findings in 21 Patients

Bone-marrow transplantation in aspartylglucosaminuria

Magnetic resonance techniques in neuronal ceroid lipofuscinoses and some other lysosomal diseases affecting the brain

Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1

Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?

Batten disease gene, CLN3 : linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes

Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI study

Aspartylglucosaminuria: Radiologic Course of the Disease With Histopathologic Correlation

Somatosensory Evoked Magnetic Fields From Primary Sensorimotor Cortex in Juvenile Neuronal Ceroid Lipofuscinosis

Jansky-Bielschowsky variant disease: CT, MRI, and SPECT findings

MRI Evaluation of the Brain in Infantile Neuronal Ceroid-Lipofuscinosis. Part 1: Postmortem MRI With Histopathologic Correlation

Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi

MRI Of the Brain, EEG Sleep Spindles and SPECT in the Early Diagnosis of Infantile Neuronal Ceroid Lipofuscinosis

DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1)

Strategy for mutation detection in CLN3: characterisation of two Finnish mutations

Antioxidant treatment in Spielmeyer-Sjögren's disease

Can barbiturate anaesthesia cure infantile spasms?

Suchergebnisse filtern