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...

Professional Tennis Players and their subsceptibility for Obsessive-Compulsive and Depressive Symptoms

European psychiatry, 2023-03, Vol.66 (S1), p.S926-S926

Cappellato, G

2023

Volltextzugriff (PDF)

Serotonin, insulin, leptin and glycolipid metabolic factor’s relationship in obesity

European psychiatry, 2023-03, Vol.66 (S1), p.S422-S423

2023

Volltextzugriff (PDF)

OP0197 POST-TRAUMATIC STRESS DISORDER AND SYMPTOMS IN PATIENTS WITH RHEUMATIC AND MUSCULOSKELETAL DISEASES DURING THE COVID-19 PANDEMIC: PRELIMINARY RESULTS FROM THE PERMAS STUDY

Annals of the rheumatic diseases, 2022-06, Vol.81 (Suppl 1), p.130-131

2022

Volltextzugriff (PDF)

Can a drug-induced pulmonary hypersensitivity reaction be dose-dependent? A case with mesalamine

The Mount Sinai journal of medicine, 2001-11, Vol.68 (6), p.389-395

2001

Volltextzugriff (PDF)

Vitamin B12, homocysteine and folic acid in obsessive-compulsive disorder

Neuroscience Applied, 2023, Vol.2, p.103450, Article 103450

2023

Volltextzugriff (PDF)

Prevention of hepatitis C virus infection in a haemodialysis centre

Nephrology, dialysis, transplantation, 1996-07, Vol.11 (7), p.1490-1491

1996

Volltextzugriff (PDF)

Post-traumatic stress disorders – latest targets for future pharmacological interventions

Neuroscience Applied, 2023, Vol.2, p.102540, Article 102540

2023

Volltextzugriff (PDF)

Facets of adult attachment style in patients with obsessive-compulsive disorder

Neuroscience Applied, 2022, Vol.1, p.100734, Article 100734

2022

Volltextzugriff (PDF)

The immuno-inflammatory model for obsessive-compulsive disorder: state of the art

Neuroscience Applied, 2022, Vol.1, p.100163, Article 100163

2022

Volltextzugriff (PDF)

Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency

Acta haematologica, 1986, Vol.75 (1), p.54-57

1986

Volltextzugriff (PDF)

Increased factor VIII associated activities in Cushing's syndrome: a probable hypercoagulable state

Thrombosis and haemostasis, 1982-01, Vol.47 (2), p.116-117

1982

Volltextzugriff (PDF)

Failure of L-asparaginase to decrease protein C--A possible rebound phenomenon

Thrombosis and haemostasis, 1986-10, Vol.56 (2), p.238-238

1986

Volltextzugriff (PDF)

Factor X antigen evaluation by means of a laser nephelometer in health and disease

Clinica chimica acta, 1985-05, Vol.148 (2), p.125-130

1985

Volltextzugriff (PDF)

CONGENITAL FACTOR XIII DEFICIENCY: TYPE I AND TYPE II DISEASE

British journal of haematology, 1985-06, Vol.60 (2), p.375-376

1985

Volltextzugriff (PDF)

Factor X Padua: a 'new' congenital factor X abnormality with a defect only in the extrinsic system

Acta haematologica, 1985, Vol.73 (1), p.31-36

1985

Volltextzugriff (PDF)

Clotting complications of L-asparaginase therapy in children with ALL

Blut, 1986-06, Vol.52 (6), p.377-378

1986

Volltextzugriff (PDF)

Antithrombin III activity and concentration in diabetes mellitus

Thrombosis and haemostasis, 1985-01, Vol.54 (2), p.415-417

1985

Volltextzugriff (PDF)

Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento)

Blut, 1986, Vol.52 (1), p.29-33

1986

Volltextzugriff (PDF)

Fibrinolytic study in plasma and ascitic fluid of cirrhotic patients before and after ascites concentration; reinfusion technique

European journal of clinical investigation, 1985-08, Vol.15 (4), p.161-165

1985

Volltextzugriff (PDF)

Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and "true" prothrombin deficiency

Blood, 1978-07, Vol.52 (1), p.115-125

1978

Volltextzugriff (PDF)

Another Family with the Factor VII Padua Clotting Defect

Acta haematologica, 1979, Vol.62 (1), p.4-11

1979

Volltextzugriff (PDF)

Study of brain capillary neuronal regulation as a tool to investigate cerebral asymmetries

Functional neurology, 1986-04, Vol.1 (2), p.105

1986

Volltextzugriff (PDF)

Antithrombin III Trento. A 'new' congenital AT III abnormality with a peculiar crossed-immunoelectrophoretic pattern in the absence of heparin

Acta haematologica, 1984, Vol.72 (2), p.73

1984

Volltextzugriff (PDF)

Type I and type II disease in congenital factor XIII deficiency. A further demonstration of the correctness of the classification

Blut, 1986-11, Vol.53 (5), p.411-413

1986

Volltextzugriff (PDF)

Rarer quantitative and qualitative abnormalities of coagulation

Clinics in haematology, 1985-06, Vol.14 (2), p.385-411

1985

Volltextzugriff (PDF)

1 – 25 von 63

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(32)

Publikationsform

Sprache

Englisch
(60)
Italienisch
(3)

Erscheinungsjahr

n.n

Thema

Humans
(43)
Science & Technology
(34)
Life Sciences & Biomedicine
(30)
Female
(23)
Hematology
(20)
Male
(17)
Biological And Medical Sciences
(16)
Adult
(15)
Medical Sciences
(15)
Pedigree
(10)
Blood Coagulation Tests
(9)
Middle Aged
(9)
Child
(8)
Antigens - Analysis
(7)
Hematologic And Hematopoietic Diseases
(6)
Heterozygote
(6)
Immunoelectrophoresis
(6)
Platelet Diseases And Coagulopathies
(6)
Aged
(5)
Cardiovascular System & Cardiology
(5)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Professional Tennis Players and their subsceptibility for Obsessive-Compulsive and Depressive Symptoms

Serotonin, insulin, leptin and glycolipid metabolic factor’s relationship in obesity

OP0197 POST-TRAUMATIC STRESS DISORDER AND SYMPTOMS IN PATIENTS WITH RHEUMATIC AND MUSCULOSKELETAL DISEASES DURING THE COVID-19 PANDEMIC: PRELIMINARY RESULTS FROM THE PERMAS STUDY

Can a drug-induced pulmonary hypersensitivity reaction be dose-dependent? A case with mesalamine

Vitamin B12, homocysteine and folic acid in obsessive-compulsive disorder

Prevention of hepatitis C virus infection in a haemodialysis centre

Post-traumatic stress disorders – latest targets for future pharmacological interventions

Facets of adult attachment style in patients with obsessive-compulsive disorder

The immuno-inflammatory model for obsessive-compulsive disorder: state of the art

Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency

Increased factor VIII associated activities in Cushing's syndrome: a probable hypercoagulable state

Failure of L-asparaginase to decrease protein C--A possible rebound phenomenon

Factor X antigen evaluation by means of a laser nephelometer in health and disease

CONGENITAL FACTOR XIII DEFICIENCY: TYPE I AND TYPE II DISEASE

Factor X Padua: a 'new' congenital factor X abnormality with a defect only in the extrinsic system

Clotting complications of L-asparaginase therapy in children with ALL

Antithrombin III activity and concentration in diabetes mellitus

Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento)

Fibrinolytic study in plasma and ascitic fluid of cirrhotic patients before and after ascites concentration; reinfusion technique

Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and "true" prothrombin deficiency

Another Family with the Factor VII Padua Clotting Defect

Study of brain capillary neuronal regulation as a tool to investigate cerebral asymmetries

Antithrombin III Trento. A 'new' congenital AT III abnormality with a peculiar crossed-immunoelectrophoretic pattern in the absence of heparin

Type I and type II disease in congenital factor XIII deficiency. A further demonstration of the correctness of the classification

Rarer quantitative and qualitative abnormalities of coagulation

Suchergebnisse filtern