Genetic abnormalities of the fibrinolytic system

A new therapeutic method for chronic subdural hematoma in adults: replacement of the hematoma with oxygen via percutaneous subdural tapping.

Surgical neurology·1992

[A case of pulmonary alveolar proteinosis and disseminated atypical mycobacteriosis complicating chronic myelogenous leukemia].

Nihon Kyobu Shikkan Gakkai zasshi·1992

Frequent rearrangements of retinoic acid receptor alpha gene and myl gene, and rare mutations of RAS and FMS genes in acute promyelocytic leukemia.

American journal of hematology·1992

Pseudoaneurysm of coronary artery following rupture of coronary artery during coronary angioplasty.

Catheterization and cardiovascular diagnosis·1992

Detection of JC virus in the brains of aged patients without progressive multifocal leukoencephalopathy by the polymerase chain reaction and Southern hybridization analysis.

Neuroscience letters·1992

Cardiac metastasis of lung cancer. A study of metastatic pathways and clinical manifestations.

Cancer·1992

Thromboelastography Parameters Thresholds for Optimal Prediction of Major Bleeding after On-Pump Cardiac Surgery.

Seminars in thrombosis and hemostasis·2026

The Historical Painting of the "Bleeding Woman": Its Relevance for Today and the Future.

Seminars in thrombosis and hemostasis·2026

Extended Anticoagulation Therapy with Rivaroxaban for Cancer-Associated Low-Risk Pulmonary Embolism According to Status of Concomitant Deep Vein Thrombosis: Insights from the ONCO PE Randomized Trial.

Seminars in thrombosis and hemostasis·2026

The evolving knowledge on primary hemostasis in neonates.

Seminars in thrombosis and hemostasis·2026

Interim Efficacy Analysis of Different Anticoagulation Regimens in Patients with Long-Term Implantation of Inferior Vena Cava Filter.

Seminars in thrombosis and hemostasis·2026

PAI-1 as a Therapeutic Target: A State-of-the-Art Review.

Seminars in thrombosis and hemostasis·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

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Genetic abnormalities of the fibrinolytic system

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A new therapeutic method for chronic subdural hematoma in adults: replacement of the hematoma with oxygen via percutaneous subdural tapping.

[A case of pulmonary alveolar proteinosis and disseminated atypical mycobacteriosis complicating chronic myelogenous leukemia].

Frequent rearrangements of retinoic acid receptor alpha gene and myl gene, and rare mutations of RAS and FMS genes in acute promyelocytic leukemia.

Pseudoaneurysm of coronary artery following rupture of coronary artery during coronary angioplasty.

Detection of JC virus in the brains of aged patients without progressive multifocal leukoencephalopathy by the polymerase chain reaction and Southern hybridization analysis.

Cardiac metastasis of lung cancer. A study of metastatic pathways and clinical manifestations.

Thromboelastography Parameters Thresholds for Optimal Prediction of Major Bleeding after On-Pump Cardiac Surgery.

The Historical Painting of the "Bleeding Woman": Its Relevance for Today and the Future.

Extended Anticoagulation Therapy with Rivaroxaban for Cancer-Associated Low-Risk Pulmonary Embolism According to Status of Concomitant Deep Vein Thrombosis: Insights from the ONCO PE Randomized Trial.

The evolving knowledge on primary hemostasis in neonates.

Interim Efficacy Analysis of Different Anticoagulation Regimens in Patients with Long-Term Implantation of Inferior Vena Cava Filter.

PAI-1 as a Therapeutic Target: A State-of-the-Art Review.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

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Genetic abnormalities of the fibrinolytic system

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