R. Mibashan

发表

D. Bentley, P. Green, R. Mibashan, 1989 .

The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII gene.

M. Vidaud, U. Martinowitz, D. Millar, 1990, Blood.

Localised intramesenteric haemorrhage--a recognisable syndrome in haemophilia?

P. Gishen, R. Mibashan, P. Dubbins, 1979, British medical journal.

Fetoscopy in the assessment of unexplained fetal hydrops

K. Nicolaides, C. Rodeck, I. Lange, 1985, British journal of obstetrics and gynaecology.

Cordocentesis in the investigation of fetal erythropoiesis.

K. Nicolaides, B. Thilaganathan, R. Mibashan, 1989, American journal of obstetrics and gynecology.

Erythroblastosis and reticulocytosis in anemic fetuses.

K. Nicolaides, C. Rodeck, B. Thilaganathan, 1988, American journal of obstetrics and gynecology.

PLASMA ASSAY OF FETAL FACTORS VIIIC AND IX FOR PRENATAL DIAGNOSIS OF HÆMOPHILIA

C. Rodeck, J. White, R. Mibashan, 1979, The Lancet.

Fetal haematology in rhesus isoimmunisation.

K. Nicolaides, C. Rodeck, D. Millar, 1985, British medical journal.

Prenatal diagnosis of hereditary protein C deficiency.

K. Nicolaides, C. Rodeck, D. Millar, 1985, The New England journal of medicine.

Activation of Hageman Factor (Factor XII) by Long-Chain Saturated Fatty Acids

R. Mibashan, P. Didisheim, 1963, Thrombosis and Haemostasis.

A Study of Coagulation Factor Levels in Women during Labour and in Their Newborn Infants

R. Mibashan, J. Hansen, P. Lanzkowsky, 1966, Thrombosis and Haemostasis.

The Measurement of Factor XI (Plasma Thromboplastin Antecedent)

R. Mibashan, J. Niemetz, H. L. Nossel, 1966, British journal of haematology.

ACUTE PROMYELOCYTIC LEUKEMIA WITH FIBRINOGEN AND FACTOR V DEFICIENCIES.

J. Trombold, R. Mibashan, P. Didisheim, 1964, Blood.

DUAL DIAGNOSIS OF PRENATAL HÆMOPHILIA A BY MEASUREMENT OF FETAL FACTOR VIIIC AND VIIIC ANTIGEN (VIIICAg)

C. Rodeck, R. Furlong, A. Bloom, 1980, The Lancet.

Molecular pathology of haemophilia B.

D. Bentley, P. Green, R. Mibashan, 1989, The EMBO journal.

First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13.

M. Pembrey, C. Rodeck, R. Winter, 1985, British medical journal.

Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients.

D. Bentley, R. Mibashan, F. Giannelli, 1988, Molecular biology & medicine.

The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene

D. Cooper, M. Krawczak, D. Whitmore, 1990, Human Genetics.

PRENATAL DIAGNOSIS OF GLANZMANN'S THROMBASTHENIA

K. Nicolaides, C. Rodeck, B. Coller, 1985, The Lancet.

FIRST-TRIMESTER DIAGNOSIS OF WISKOTT-ALDRICH SYNDROME BY DNA MARKERS

K. Nicolaides, C. Rodeck, M. Schwartz, 1989, The Lancet.

Recurrent intracranial haemorrhages in utero in an infant with alloimmune thrombocytopenia. Case report

G. Bydder, C. Rodeck, L. S. Vries, 1988, British journal of obstetrics and gynaecology.

FETAL HAEMOGLOBIN MEASUREMENT IN THE ASSESSMENT OF RED CELL ISOIMMUNISATION

K. Nicolaides, C. Rodeck, S. Campbell, 1988, The Lancet.

Human embryonic zeta-globin chains in fetal and newborn blood.

D. Higgs, S. Perrine, D. Chui, 1989, Blood.

Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism

D. Cooper, V. Kakkar, D. Millar, 2004, Human Genetics.

Fetal haemophilia and allied bleeding disorders.

D. Millar, R. Mibashan, 1983, British medical bulletin.

Antenatal management of fetomaternal alloimmune thrombocytopenia—report of 15 affected pregnancies

K. Nicolaides, C. Rodeck, Melissa S. Murphy, 1994, Transfusion medicine.

Prenatal diagnosis of haemophilia A and Christmas disease

C. Rodeck, R. Mibashan, 1982 .

Have Liley charts outlived their usefulness?

K. Nicolaides, C. Rodeck, R. Mibashan, 1986, American journal of obstetrics and gynecology.

Automated Control of Coumarin Therapy by Chromogenic Factor X Assay

M. Scully, I. Macgregor, R. Mibashan, 1979, Thrombosis and Haemostasis.

HAEMOPHILIA WITH A SPECIES SPECIFIC INillBITOR OF FACTOR VIII

R. Mibashan, H. L. Nossel, 1965 .

Management of Fetal Alloimmune Thrombocytopenia by Weekly in utero Platelet Transfusions

K. Nicolaides, M. Murphy, R. Mibashan, 1990, Vox sanguinis.

Normal blood cell values in the early mid‐trimester fetus

K. Nicolaides, C. Rodeck, K. Nicolaides, 1985, Prenatal diagnosis.

Selective feticide of the affected twin by fetoscopic air embolism

C. Rodeck, J. Abramowicz, R. Mibashan, 1982, Prenatal diagnosis.

Pemphigoid gestationis and neonatal alloimmune thrombocytopenia

R. Mibashan, A. du Vivier, B. Adriaans, 1990, Clinical and experimental dermatology.

FETAL PLATELET TRASFUSIONS IN THE MANAGEMENT OF ALLOIMMUNE THROMBOCYTOPENIA

K. Nicolaides, C. Rodeck, L. S. Vries, 1987, Thrombosis and Haemostasis.

Prevention program of type I Glanzmann thrombasthenia in Israel: prenatal diagnosis.

K. Nicolaides, C. Rodeck, B. Coller, 1988, Current studies in hematology and blood transfusion.

D URING HUMAN embryonic and fetal development

D. Higgs, S. Perrine, R. Mibashan, 2017 .

Carrier Detection Of Haemophilia A In Pregnancy By Measurement Of Factor VIIIc/Rag And VIIICAg/RAg Ratios

R. Newcombe, C. Rodeck, R. Furlong, 1981, Thrombosis and Haemostasis.

Effect of the choice of WHO International Reference Preparation for thromboplastin on International Normalised Ratios.

N. Shinton, J. Morris, L. Poller, 1993, Journal of clinical pathology.

Obstetric management and diagnosis of haematological disease in the fetus.

K. Nicolaides, C. Rodeck, R. Mibashan, 1985, Clinics in haematology.

Guidelines on oral anticoagulation: second edition

N. Shinton, B. Colvin, F. Preston, 1990 .

A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism.

D. Bentley, R. Mibashan, F. Giannelli, 1988, The EMBO journal.

Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus

D. Cooper, P. Jedlicka, D. Millar, 1990, Human Genetics.

Prenatal diagnosis of β thalassaemia by reverse phase HPLC

M. Vidaud, P. Rouyer‐Fessard, Y. Beuzard, 1987 .

Prenatal diagnosis of haemoglobinopathies by ion exchange hplc of haemoglobins

M. Vidaud, P. Rouyer‐Fessard, Y. Beuzard, 1989, Prenatal diagnosis.

Diagnosis and treatment of feto-maternal hemorrhage in a fetus with homozygous von Willebrand's disease.

K. Nicolaides, R. Mibashan, K. M. Ash, 1988, Fetal Therapy.