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...

Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer

Molecular genetics and metabolism, 2003-09, Vol.80 (1), p.148-158

2003

Volltextzugriff (PDF)

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern

The Journal of pediatrics, 1999-02, Vol.134 (2), p.193-198

1999

Volltextzugriff (PDF)

Sustained correction of OTC deficiency in spf( ash) mice using optimized self-complementary AAV2/8 vectors

Gene therapy, 2012-04, Vol.19 (4), p.404-410

2012

Volltextzugriff (PDF)

Alternative pathway therapy for urea cycle disorders: Twenty years later

The Journal of pediatrics, 2001-01, Vol.138 (1), p.S46-S55

2001

Volltextzugriff (PDF)

A pilot study of in vivo liver-directed gene transfer with an adenoviral vector in partial ornithine transcarbamylase deficiency

Human gene therapy, 2002-01, Vol.13 (1), p.163-175

2002

Volltextzugriff (PDF)

Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors

Gene therapy, 2000-12, Vol.7 (23), p.1986-1992

2000

Volltextzugriff (PDF)

Sustained correction of OTC deficiency in spfash mice using optimized self-complementary AAV2/8 vectors

Gene therapy, 2012-04, Vol.19 (4), p.404-410

2012

Volltextzugriff (PDF)

Cognitive outcome in urea cycle disorders

Molecular genetics and metabolism, 2004-04, Vol.81, p.58-62

2004

Volltextzugriff (PDF)

Correction of argininosuccinate synthetase (AS) deficiency in a murine model of citrullinemia with recombinant adenovirus carrying human AS cDNA

Gene therapy, 2000-10, Vol.7 (20), p.1777-1782

2000

Volltextzugriff (PDF)

Transient depletion of CD4 lymphocyte improves efficacy of repeated administration of recombinant adenovirus in the ornithine transcarbamylase deficient sparse fur mouse

Gene therapy, 2000-10, Vol.7 (20), p.1761-1767

2000

Volltextzugriff (PDF)

Inborn errors of urea synthesis

Annals of neurology, 1994-02, Vol.35 (2), p.133-141

Batshaw, Mark L.

1994

Volltextzugriff (PDF)

Recombinant adenovirus gene transfer in adults with partial ornithine transcarbamylase deficiency (OTCD)

Human gene therapy, 1999-09, Vol.10 (14), p.2419-2437

1999

Volltextzugriff (PDF)

Developing adenoviral‐mediated in vivo gene therapy for ornithine transcarbamylase deficiency

Journal of inherited metabolic disease, 1998-06, Vol.21 (S1), p.119-137

1998

Volltextzugriff (PDF)

Prolonged Metabolic Correction in Adult Ornithine Transcarbamylase-deficient Mice with Adenoviral Vectors (∗)

The Journal of biological chemistry, 1996-02, Vol.271 (7), p.3639-3646

1996

Volltextzugriff (PDF)

Down Syndrome

The Pediatric clinics of North America, 1993-06, Vol.40 (3), p.523-535

1993

Volltextzugriff (PDF)

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency

Molecular genetics and metabolism, 2008-09, Vol.95 (1), p.21-30

2008

Volltextzugriff (PDF)

Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectors

Human gene therapy, 2001-06, Vol.12 (9), p.1035-1046

2001

Volltextzugriff (PDF)

Correction of ureagenesis after gene transfer in an animal model and after liver transplantation in humans with ornithine transcarbamylase deficiency

Pediatric research, 1999-11, Vol.46 (5), p.588-593

1999

Volltextzugriff (PDF)

Adenovirus-mediated in vivo gene transfer rapidly protects ornithine transcarbamylase-deficient mice from an ammonium challenge

Pediatric research, 1997-04, Vol.41 (4), p.527-534

1997

Volltextzugriff (PDF)

Quinolinic acid in children with congenital hyperammonemia

Annals of neurology, 1993-11, Vol.34 (5), p.676-681

1993

Volltextzugriff (PDF)

Cerebral Palsy

The Pediatric clinics of North America, 1993-06, Vol.40 (3), p.537-551

1993

Volltextzugriff (PDF)

In vivo measurement of ureagenesis with stable isotopes

Journal of inherited metabolic disease, 1998-06, Vol.21 (S1), p.21-29

1998

Volltextzugriff (PDF)

Mental Retardation

The Pediatric clinics of North America, 1993-06, Vol.40 (3), p.507-521

Batshaw, Mark L.

1993

Volltextzugriff (PDF)

Traumatic Brain Injury in Children

The Pediatric clinics of North America, 1993-06, Vol.40 (3), p.553-565

1993

Volltextzugriff (PDF)

Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia

Pediatric research, 1985-07, Vol.19 (7), p.666-671

1985

Volltextzugriff (PDF)

1 – 25 von 145

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(130)
Mit Volltextzugriff
(106)

Publikationsform

Artikel
(145)

Sprache

Englisch
(144)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(92)
Humans
(90)
Life Sciences & Biomedicine
(90)
Female
(60)
Male
(57)
Biological And Medical Sciences
(47)
Medical Sciences
(43)
Pediatrics
(38)
Ammonia - Blood
(37)
Animals
(34)
Infant, Newborn
(34)
Infant
(31)
Ornithine Carbamoyltransferase Deficiency Disease
(27)
Child
(26)
Child, Preschool
(26)
Genetics & Heredity
(26)
Mice
(24)
Medicine, Research & Experimental
(23)
Research & Experimental Medicine
(23)
Adult
(22)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern

Sustained correction of OTC deficiency in spf( ash) mice using optimized self-complementary AAV2/8 vectors

Alternative pathway therapy for urea cycle disorders: Twenty years later

A pilot study of in vivo liver-directed gene transfer with an adenoviral vector in partial ornithine transcarbamylase deficiency

Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors

Sustained correction of OTC deficiency in spfash mice using optimized self-complementary AAV2/8 vectors

Cognitive outcome in urea cycle disorders

Correction of argininosuccinate synthetase (AS) deficiency in a murine model of citrullinemia with recombinant adenovirus carrying human AS cDNA

Transient depletion of CD4 lymphocyte improves efficacy of repeated administration of recombinant adenovirus in the ornithine transcarbamylase deficient sparse fur mouse

Inborn errors of urea synthesis

Recombinant adenovirus gene transfer in adults with partial ornithine transcarbamylase deficiency (OTCD)

Developing adenoviral‐mediated in vivo gene therapy for ornithine transcarbamylase deficiency

Prolonged Metabolic Correction in Adult Ornithine Transcarbamylase-deficient Mice with Adenoviral Vectors (∗)

Down Syndrome

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency

Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectors

Correction of ureagenesis after gene transfer in an animal model and after liver transplantation in humans with ornithine transcarbamylase deficiency

Adenovirus-mediated in vivo gene transfer rapidly protects ornithine transcarbamylase-deficient mice from an ammonium challenge

Quinolinic acid in children with congenital hyperammonemia

Cerebral Palsy

In vivo measurement of ureagenesis with stable isotopes

Mental Retardation

Traumatic Brain Injury in Children

Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia

Suchergebnisse filtern