UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 26

Sortiert nach

Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GP1) deficiency

Human genetics, 1998-10, Vol.103 (4), p.450-454

1998

Volltextzugriff (PDF)

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia

Human genetics, 1994-11, Vol.94 (5), p.560-562

1994

Volltextzugriff (PDF)

A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova): biochemical characterization and mosaicism expression in the heterozygote

Human genetics, 1990-03, Vol.84 (4), p.337-340

1990

Volltextzugriff (PDF)

Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP): molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum

Human genetics, 1989, Vol.81 (2), p.161-164

1989

Volltextzugriff (PDF)

G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia

Human genetics, 1982-01, Vol.61 (2), p.175-176

1982

Volltextzugriff (PDF)

Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients

Human genetics, 1980-03, Vol.53 (3), p.401-408

1980

Volltextzugriff (PDF)

Glucose 6-phosphate dehydrogenase variants: a unique variant (G6PD Kobe) showed an extremely increased affinity for galactose 6-phosphate and a new variant (G6PD Sapporo) resembling G6PD Pea Ridge

Human genetics, 1981-10, Vol.58 (4), p.405-407

1981

Volltextzugriff (PDF)

Pyruvate kinase "Göttingen 1,2": congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity

Human genetics, 1982, Vol.60 (4), p.381-386

1982

Volltextzugriff (PDF)

Three cases of hereditary hemolytic anemia with pyrimidine 5'-nucleotidase deficiency in a Japanese family

Human genetics, 1977-07, Vol.37 (3), p.361-364

1977

Volltextzugriff (PDF)

G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia

Human genetics, 1982-01, Vol.62 (2), p.110-112

1982

Volltextzugriff (PDF)

Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita

Human genetics, 1978-11, Vol.45 (1), p.11-17

1978

Volltextzugriff (PDF)

Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France

Human genetics, 1980-07, Vol.55 (1), p.125-127

1980

Volltextzugriff (PDF)

The detection of heterozygous G6PD deficiency; similarity between glutathione deficiency and G6PD deficiency

Human genetics, 1970-01, Vol.9 (3), p.254-255

Prins, H K

1970

Volltextzugriff (PDF)

The polymorphism of nucleosid effect in pyruvate kinase deficiency

Human genetics, 1970-01, Vol.9 (3), p.257-259

1970

Volltextzugriff (PDF)

PGI3(Israel), a new, unstable allele in the phosphoglucose isomerase system

Human genetics, 1987-09, Vol.77 (1), p.76-79

1987

Volltextzugriff (PDF)

Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an Italian family

Human genetics, 1981-01, Vol.57 (2), p.226-229

1981

Volltextzugriff (PDF)

Characterization of a series of electrophoretic and enzyme activity variants of human glucose-phosphate isomerase

Human genetics, 1987, Vol.75 (1), p.28-31

1987

Volltextzugriff (PDF)

G6PD Sendagi: a new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia

Human genetics, 1983-01, Vol.65 (2), p.214-215

1983

Volltextzugriff (PDF)

Advances in hereditary red cell enzyme anomalies

Human genetics, 1979-01, Vol.50 (1), p.1-27

1979

Volltextzugriff (PDF)

Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: clinical and familial studies

Human genetics, 1975-10, Vol.29 (4), p.291-297

1975

Volltextzugriff (PDF)

Molecular and functional anomalies in two new mutant glucose-phosphate-insomerase variants with enzyme deficiency and chronic hemolysis

Human genetics, 1978-02, Vol.40 (3), p.293-304

1978

Volltextzugriff (PDF)

Molecular mechanism of erythrocyte pyruvate kinase deficiency

Human genetics, 1975-10, Vol.29 (4), p.271-280

1975

Volltextzugriff (PDF)

'Gd(-) Hôtel Dieu': a new G-6PD variant with chronic hemolysis in a Negro patient from Senegal

Human genetics, 1977-12, Vol.39 (3), p.353-357

1977

Volltextzugriff (PDF)

Hereditary hemolytic anemia with erythrocyte phosphofructokinase deficiency: studies of some properties of erythrocyte and muscle enzyme

Human genetics, 1976-01, Vol.31 (1), p.83-91

1976

Volltextzugriff (PDF)

Genetic variability of G-6-PD

Human genetics, 1970-01, Vol.9 (3), p.250-252

Beutler, E

1970

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Aktive Filter

SpracheDeutsch

Zeitschrift / SerieHuman Genetics

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(26)
Mit Volltextzugriff
(26)

Publikationsform

Artikel
(26)

Sprache

Englisch
(26)

Erscheinungsjahr

n.n

Kollektion

MEDLINE
(26)
Springer journals
(26)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(25)
Ingenta
(25)

Zeitschrift / Serie

Humangenetik
(6)

Menü

Weitere Dienste

Einstellungen

Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GP1) deficiency

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia

A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova): biochemical characterization and mosaicism expression in the heterozygote

Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP): molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum

G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia

Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients

Glucose 6-phosphate dehydrogenase variants: a unique variant (G6PD Kobe) showed an extremely increased affinity for galactose 6-phosphate and a new variant (G6PD Sapporo) resembling G6PD Pea Ridge

Pyruvate kinase "Göttingen 1,2": congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity

Three cases of hereditary hemolytic anemia with pyrimidine 5'-nucleotidase deficiency in a Japanese family

G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia

Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita

Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France

The detection of heterozygous G6PD deficiency; similarity between glutathione deficiency and G6PD deficiency

The polymorphism of nucleosid effect in pyruvate kinase deficiency

PGI3(Israel), a new, unstable allele in the phosphoglucose isomerase system

Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an Italian family

Characterization of a series of electrophoretic and enzyme activity variants of human glucose-phosphate isomerase

G6PD Sendagi: a new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia

Advances in hereditary red cell enzyme anomalies

Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: clinical and familial studies

Molecular and functional anomalies in two new mutant glucose-phosphate-insomerase variants with enzyme deficiency and chronic hemolysis

Molecular mechanism of erythrocyte pyruvate kinase deficiency

'Gd(-) Hôtel Dieu': a new G-6PD variant with chronic hemolysis in a Negro patient from Senegal

Hereditary hemolytic anemia with erythrocyte phosphofructokinase deficiency: studies of some properties of erythrocyte and muscle enzyme

Genetic variability of G-6-PD

Aktive Filter

Suchergebnisse filtern