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Publications by Dusan Loderer

Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia

Seminars in Thrombosis and Hemostasis
Cardiovascular MedicineHematologyCardiology
2016English

Novel Fibrinogen Bbeta Chain Mutation as an Underlying Mechanism of Afibrinogenemia?

Seminars in Thrombosis and Hemostasis
Cardiovascular MedicineHematologyCardiology
2015English

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Congenital Afibrinogenemia: First Identification of Splicing Mutations in the Fibrinogen Bbeta -Chain Gene Causing Activation of Cryptic Splice Sites

Blood
BiochemistryImmunologyCell BiologyHematology
2002English

Congenital Afibrinogenemia

Annals of Saudi Medicine
Medicine
2000English

A Still Rare Case of Congenital Afibrinogenemia

Journal of Clinical & Experimental Immunology
2018English

A Novel Mutation in the TG Gene (G2322S) Causing Congenital Hypothyroidism in a Sudanese Family: A Case Report

BMC Medical Genetics
Genetics
2018English

Severe Elbow Arthropathy in a Patient With Congenital Afibrinogenemia

Journal of Bone and Joint Surgery - Series A
MedicineSurgeryOrthopedicsSports MedicineSports Science
2010English

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in Pediatrics
Child HealthPediatricsPerinatology
2017English

Novel Mutation in KCNQ2 Causing Ohtahara Syndrome

Annals of Child Neurology
2019English

A Novel SERPINA1 Mutation Causing Serum Alpha1-Antitrypsin Deficiency

PLoS ONE
Multidisciplinary
2012English

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