UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 182

Sortiert nach

MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation

Canadian journal of neurological sciences, 2014-03, Vol.41 (2), p.210-219

2014

Volltextzugriff (PDF)

Extensively coated femoral components in young patients

Clinical orthopaedics and related research, 1997-11, Vol.344 (344), p.263-274

1997

Volltextzugriff (PDF)

Prenatal diagnosis by amniocentesis and chorionic villus biopsy of mtDNA mutation 8993T>G

Journal of inherited metabolic disease, 2007-06, Vol.30 (3), p.404-404

2007

Volltextzugriff (PDF)

Arthroplasty-associated malignant fibrous histiocytoma: two case reports

Histopathology, 2001-12, Vol.39 (6), p.620-628

2001

Volltextzugriff (PDF)

Achieving the “triple aim” for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework

Genetics in medicine, 2013-06, Vol.15 (6), p.415-422

2013

Volltextzugriff (PDF)

Total joint arthroplasty and the immune response

Seminars in arthritis and rheumatism, 1997-08, Vol.27 (1), p.44-47

1997

Volltextzugriff (PDF)

Extended proximal femoral osteotomy

Instructional course lectures, 1999, Vol.48, p.19

1999

Volltextzugriff (PDF)

In memoriam. collaborative research and the misuse of genetics: a memorial to William Marks

The Journal of heredity, 1999-01, Vol.90 (1), p.263-264

1999

Volltextzugriff (PDF)

A portable nitric oxide scavenging system designed for use on neonatal transport

Critical care medicine, 1996-06, Vol.24 (6), p.1068-1071

1996

Volltextzugriff (PDF)

Influence of referring physicians on interventions by a pediatric and neonatal critical care transport team

Pediatric emergency care, 1996-04, Vol.12 (2), p.73-77

1996

Volltextzugriff (PDF)

Teratogenic effects of ethyl alcohol administered to pregnant mice

American journal of obstetrics and gynecology, 1976-04, Vol.124 (7), p.676-680

Kronick, J.B.

1976

Volltextzugriff (PDF)

The Gy Mutation: Another Cause of X-Linked Hypophosphatemia in Mouse

Proceedings of the National Academy of Sciences - PNAS, 1986-07, Vol.83 (13), p.4899-4903

1986

Volltextzugriff (PDF)

Jugular venous bulb catheterization in infants and children

Critical care medicine, 1989-05, Vol.17 (5), p.385-388

1989

Volltextzugriff (PDF)

Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria

American journal of medical genetics. Part A, 2005-06, Vol.135A (3), p.289-291

2005

Volltextzugriff (PDF)

Nephrocalcinosis and its relationship to treatment of hereditary rickets

The Journal of pediatrics, 1987-11, Vol.111 (5), p.700-704

1987

Volltextzugriff (PDF)

3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

Journal of inherited metabolic disease, 1992-01, Vol.15 (2), p.204-212

1992

Volltextzugriff (PDF)

Pediatric and neonatal critical care transport: A comparison of therapeutic interventions

Pediatric emergency care, 1996-02, Vol.12 (1), p.23-26

1996

Volltextzugriff (PDF)

Acute respiratory failure mediated by reactive drug metabolites

Biology of the neonate, 1995, Vol.67 (4), p.223

1995

Volltextzugriff (PDF)

Psychogenic upper airway obstruction

Pediatrics (Evanston), 1988-05, Vol.81 (5), p.714

1988

Volltextzugriff (PDF)

Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap

Molecular genetics and metabolism, 2003-05, Vol.79 (1), p.6-16

2003

Volltextzugriff (PDF)

The Expanding Spectrum of Medium Chain Acyl-Coenzyme a Dehydrogenase Deficiency (Mcadd) from Trait to Lethality: Mcadd Experience Using the Canadian Paediatric Surveillance Program

Paediatrics & child health, 2009-05, Vol.14 (suppl_A), p.26-26A

2009

Volltextzugriff (PDF)

Guidelines for stabilizing the condition of the critically ill child before transfer to a tertiary care facility

Canadian Medical Association journal (CMAJ), 1988-08, Vol.139 (3), p.213

1988

Volltextzugriff (PDF)

The Hartnup phenotype: Mendelian transport disorder, multifactorial disease

American journal of human genetics, 1987-05, Vol.40 (5), p.401-412

1987

Volltextzugriff (PDF)

Relationship of cross-brain oxygen content difference, cerebral blood flow, and metabolic rate to neurologic outcome after near-drowning

The Journal of pediatrics, 1992-12, Vol.121 (6), p.839-844

1992

Volltextzugriff (PDF)

Role of transcutaneous pacing in the setting of a failing permanent pacemaker

Pediatric emergency care, 1989-09, Vol.5 (3), p.178-180

1989

Volltextzugriff (PDF)

1 – 25 von 182

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(162)
Mit Volltextzugriff
(152)

Publikationsform

Artikel
(159)
Reviews
(18)
Buchkapitel
(4)
Bücher
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation

Extensively coated femoral components in young patients

Prenatal diagnosis by amniocentesis and chorionic villus biopsy of mtDNA mutation 8993T>G

Arthroplasty-associated malignant fibrous histiocytoma: two case reports

Achieving the “triple aim” for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework

Total joint arthroplasty and the immune response

Extended proximal femoral osteotomy

In memoriam. collaborative research and the misuse of genetics: a memorial to William Marks

A portable nitric oxide scavenging system designed for use on neonatal transport

Influence of referring physicians on interventions by a pediatric and neonatal critical care transport team

Teratogenic effects of ethyl alcohol administered to pregnant mice

The Gy Mutation: Another Cause of X-Linked Hypophosphatemia in Mouse

Jugular venous bulb catheterization in infants and children

Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria

Nephrocalcinosis and its relationship to treatment of hereditary rickets

3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

Pediatric and neonatal critical care transport: A comparison of therapeutic interventions

Acute respiratory failure mediated by reactive drug metabolites

Psychogenic upper airway obstruction

Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap

The Expanding Spectrum of Medium Chain Acyl-Coenzyme a Dehydrogenase Deficiency (Mcadd) from Trait to Lethality: Mcadd Experience Using the Canadian Paediatric Surveillance Program

Guidelines for stabilizing the condition of the critically ill child before transfer to a tertiary care facility

The Hartnup phenotype: Mendelian transport disorder, multifactorial disease

Relationship of cross-brain oxygen content difference, cerebral blood flow, and metabolic rate to neurologic outcome after near-drowning

Role of transcutaneous pacing in the setting of a failing permanent pacemaker

Suchergebnisse filtern