UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.715

Sortiert nach

Diagnosis of adenine phosphoribosyltransferase deficiency as the underlying cause of renal failure in a renal transplant recipient

Nephrology, dialysis, transplantation, 2004-03, Vol.19 (3), p.736-738

2004

Volltextzugriff (PDF)

Effect of methotrexate on blood purine and pyrimidine levels in patients with rheumatoid arthritis

Rheumatology (Oxford, England), 1999-10, Vol.38 (10), p.997-1002

1999

Volltextzugriff (PDF)

Chronic hemolytic anemia and accumulation of pyrimidine nucleotide metabolites

International journal of laboratory hematology, 2015-08, Vol.37 (4), p.e72-e74

2015

Volltextzugriff (PDF)

Severe Impairment of Nucleotide Synthesis Through Inhibition of Mitochondrial Respiration

Nucleosides, nucleotides & nucleic acids, 2004-10, Vol.23 (8-9), p.1275-1279

2004

Volltextzugriff (PDF)

Early treatment with allopurinol in familial juvenile hyerpuricaemic nephropathy (FJHN) ameliorates the long‐term progression of renal disease

QJM : An International Journal of Medicine, 2002-09, Vol.95 (9), p.597-607

2002

Volltextzugriff (PDF)

Gout, uric acid and purine metabolism in paediatric nephrology

Pediatric nephrology (Berlin, West), 1993-02, Vol.7 (1), p.105-118

1993

Volltextzugriff (PDF)

Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency

Human genetics, 2002-10, Vol.111 (4-5), p.360-367

2002

Volltextzugriff (PDF)

Dedication to Francoise Roch-Ramel

Nucleosides, nucleotides & nucleic acids, 2004-10, Vol.23 (8-9), p.1081-1082

Simmonds, H. A.

2004

Volltextzugriff (PDF)

4-pyridone-3-carboxamide ribonucleoside triphosphate accumulating in erythrocytes in end stage renal failure originates from tryptophan metabolism

Clinical and experimental medicine, 2007-12, Vol.7 (4), p.135-141

2007

Volltextzugriff (PDF)

Adenine Phosphoribosyltransferase-Deficient Mice Develop 2,8-Dihydroxyadenine Nephrolithiasis

Proceedings of the National Academy of Sciences - PNAS, 1996-05, Vol.93 (11), p.5307-5312

1996

Volltextzugriff (PDF)

Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning

Bone marrow transplantation (Basingstoke), 2001-07, Vol.28 (1), p.93-96

2001

Volltextzugriff (PDF)

The importance of thiopurine methyltransferase activity for the use of azathioprine in transplant recipients

Transplantation, 1992, Vol.53 (5), p.1051

1992

Volltextzugriff (PDF)

When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indications

Journal of inherited metabolic disease, 1997-06, Vol.20 (2), p.214-226

1997

Volltextzugriff (PDF)

Familial Juvenile Hyperuricaemic Nephropathy is not Such a Rare Genetic Metabolic Purine Disease in Britain

Nucleosides, nucleotides & nucleic acids, 2006-01, Vol.25 (9-11), p.1071-1075

2006

Volltextzugriff (PDF)

Importance of ribonucleotide availability to proliferating T-lymphocytes from healthy humans. Disproportionate expansion of pyrimidine pools and contrasting effects of de novo synthesis inhibitors

The Journal of biological chemistry, 1995-12, Vol.270 (50), p.29682-29689

1995

Volltextzugriff (PDF)

Leflunomide Inhibits Pyrimidine de Novo Synthesis in Mitogen-stimulated T-lymphocytes from Healthy Humans

The Journal of biological chemistry, 1998-08, Vol.273 (34), p.21682-21691

1998

Volltextzugriff (PDF)

The Novel Nucleotide 4KNTP, in High Concentrations in Erythrocytes of Renal Failure Children: a Comparison with Accumulation of Other Putative Precursors in the Plasma

Nucleosides, nucleotides & nucleic acids, 2006-01, Vol.25 (9-11), p.1051-1054

2006

Volltextzugriff (PDF)

Low-dose allopurinol plus azathioprine/ cyclosporin/prednisolone, a novel immunosuppressive regimen

The Lancet (British edition), 1993-07, Vol.342 (8863), p.83-84

1993

Volltextzugriff (PDF)

Adult presentation of adenosine deaminase deficiency

The Lancet (British edition), 1993-06, Vol.341 (8858), p.1471-1471

1993

Volltextzugriff (PDF)

Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency

Blood, 1996-10, Vol.88 (7), p.2761-2767

1996

Volltextzugriff (PDF)

HPLC determination of oxidized and reduced pyridine coenzymes in human erythrocytes

Clinica chimica acta, 1993-10, Vol.220 (1), p.1-17

1993

Volltextzugriff (PDF)

HPRT-APRT-deficient Mice Are Not a Model for Lesch-Nyhan Syndrome

Human molecular genetics, 1996-10, Vol.5 (10), p.1607-1610

1996

Volltextzugriff (PDF)

Diagnosis of molybdenum cofactor deficiency

The Lancet (British edition), 1999-02, Vol.353 (9153), p.675-675

1999

Volltextzugriff (PDF)

Familial juvenile hyperuricaemic nephropathy

QJM : An International Journal of Medicine, 2004-02, Vol.97 (2), p.106-107

2004

Volltextzugriff (PDF)

Presymptomatic detection of familial juvenile hyperuricaemic nephropathy in children

Pediatric nephrology (Berlin, West), 1998-06, Vol.12 (5), p.357-364

1998

Volltextzugriff (PDF)

1 – 25 von 1.715

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.482)
Mit Volltextzugriff
(1.325)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(966)
Life Sciences & Biomedicine
(789)
Humans
(669)
Male
(329)
Female
(315)
Biological And Medical Sciences
(282)
Medical Sciences
(205)
Adult
(190)
Animals
(186)
Physical Sciences
(162)
Middle Aged
(145)
Child
(107)
Medicine, Research & Experimental
(100)
Research & Experimental Medicine
(98)
Fundamental And Applied Biological Sciences. Psychology
(95)
Virology
(95)
Aged
(94)
Biochemistry & Molecular Biology
(88)
Infectious Diseases
(88)
Adolescent
(81)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Diagnosis of adenine phosphoribosyltransferase deficiency as the underlying cause of renal failure in a renal transplant recipient

Effect of methotrexate on blood purine and pyrimidine levels in patients with rheumatoid arthritis

Chronic hemolytic anemia and accumulation of pyrimidine nucleotide metabolites

Severe Impairment of Nucleotide Synthesis Through Inhibition of Mitochondrial Respiration

Early treatment with allopurinol in familial juvenile hyerpuricaemic nephropathy (FJHN) ameliorates the long‐term progression of renal disease

Gout, uric acid and purine metabolism in paediatric nephrology

Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency

Dedication to Francoise Roch-Ramel

4-pyridone-3-carboxamide ribonucleoside triphosphate accumulating in erythrocytes in end stage renal failure originates from tryptophan metabolism

Adenine Phosphoribosyltransferase-Deficient Mice Develop 2,8-Dihydroxyadenine Nephrolithiasis

Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning

The importance of thiopurine methyltransferase activity for the use of azathioprine in transplant recipients

When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indications

Familial Juvenile Hyperuricaemic Nephropathy is not Such a Rare Genetic Metabolic Purine Disease in Britain

Importance of ribonucleotide availability to proliferating T-lymphocytes from healthy humans. Disproportionate expansion of pyrimidine pools and contrasting effects of de novo synthesis inhibitors

Leflunomide Inhibits Pyrimidine de Novo Synthesis in Mitogen-stimulated T-lymphocytes from Healthy Humans

The Novel Nucleotide 4KNTP, in High Concentrations in Erythrocytes of Renal Failure Children: a Comparison with Accumulation of Other Putative Precursors in the Plasma

Low-dose allopurinol plus azathioprine/ cyclosporin/prednisolone, a novel immunosuppressive regimen

Adult presentation of adenosine deaminase deficiency

Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency

HPLC determination of oxidized and reduced pyridine coenzymes in human erythrocytes

HPRT-APRT-deficient Mice Are Not a Model for Lesch-Nyhan Syndrome

Diagnosis of molybdenum cofactor deficiency

Familial juvenile hyperuricaemic nephropathy

Presymptomatic detection of familial juvenile hyperuricaemic nephropathy in children

Suchergebnisse filtern