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Hereditary Breast Cancer in Romania-Molecular Particularities and Genetic Counseling Challenges in an Eastern European Country

Biomedicines, 2023-05, Vol.11 (5), p.1386

2023

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The C677T Variant in the Methylenetetrahydrofolate Reductase Gene and Idiopathic Spontaneous Abortion in a Romanian Population Group

Notulae scientia biologicae, 2012-02, Vol.4 (1), p.7-11

2012

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The relationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia

Annals of hematology, 2014-02, Vol.93 (2), p.203-209

2014

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Cytogenetic and fragile X testing in a group of Romanian autistic children

Human & veterinary medicine, 2015-12, Vol.7 (4), p.276-282

2015

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G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms

Annals of hematology, 2010-10, Vol.89 (10), p.979-983

2010

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TLR1 polymorphisms in Europeans and spontaneous pregnancy loss

Gene, 2012-02, Vol.494 (1), p.109-111

2012

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Absence of BRAF V600E mutation in a cohort of 402 patients with various chronic and acute myeloid neoplasms

Leukemia & lymphoma, 2012-12, Vol.53 (12), p.2496-2497

2012

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No association between the STAT5b rs6503691 (C>T) SNP and myeloproliferative neoplasms

European journal of haematology, 2013-03, Vol.90 (3), p.257-258

2013

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Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report

Journal of gastrointestinal and liver diseases : JGLD, 2010-06, Vol.19 (2), p.191-193

2010

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Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

Indian journal of hematology & blood transfusion, 2014-09, Vol.30 (Suppl 1), p.120-123

2014

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CALR versus JAK2 mutated essential thrombocythaemia - a report on 141 patients

British journal of haematology, 2015-01, Vol.168 (1), p.151-153

2015

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HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania

Journal of gastrointestinal and liver diseases : JGLD, 2012-06, Vol.21 (2), p.177

2012

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CALR versus JAK2 mutated essential thrombocythaemia – a report on 141 patients

British journal of haematology, 2015-01, Vol.168 (1), p.151-153

2015

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CALR versus JAK 2 mutated essential thrombocythaemia – a report on 141 patients

British journal of haematology, 2015-01, Vol.168 (1), p.151-153

2015

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No association between the STAT 5b rs6503691 (C>T) SNP and myeloproliferative neoplasms

European journal of haematology, 2013-03, Vol.90 (3), p.257-258

2013

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The G allele of the rs10974944 SNP, part of 46/1 haplotype, is strongly associated with V617F-positive myeloproliferative neoplasms

Annals of hematology, 2010-04, Vol.89 (10), p.979-983

2010

Volltextzugriff (PDF)

Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

Indian journal of hematology & blood transfusion, 2013-06, Vol.30 (Suppl 1), p.120-123

2013

Volltextzugriff (PDF)

The C677T Variant in the Methylenetetrahydrofolate Reductase Gene and Idiopathic Spontaneous Abortion in a Romanian Population Group

Notulae scientia biologicae, 2012-02, Vol.4 (1), p.07-11

2012

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Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 2014, Vol.30, p.120-123

2014

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Molecular basis and therapeutic targets in prostate cancer: A comprehensive review

Biomolecules & biomedicine, 2023-10, Vol.23 (5), p.760-771

2023

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Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array

Journal of personalized medicine, 2024-03, Vol.14 (3), p.290

2024

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The Impact of Chromosomal Mosaicisms on Prenatal Diagnosis and Genetic Counseling—A Narrative Review

Journal of personalized medicine, 2024-07, Vol.14 (7), p.774

2024

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Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive Review

Medicina (Kaunas, Lithuania), 2024-05, Vol.60 (5), p.767

2024

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A comprehensive review on the molecular basis and therapeutic targets in prostate cancer

Biomolecules & biomedicine, 2023-04

2023

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Challenging diagnoses of tetraploidy/diploidy and trisomy 12: utility of first-tier prenatal testing methods

Frontiers in genetics, 2023-11, Vol.14, p.1258752-1258752

2023

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Hereditary Breast Cancer in Romania-Molecular Particularities and Genetic Counseling Challenges in an Eastern European Country

The C677T Variant in the Methylenetetrahydrofolate Reductase Gene and Idiopathic Spontaneous Abortion in a Romanian Population Group

The relationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia

Cytogenetic and fragile X testing in a group of Romanian autistic children

G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms

TLR1 polymorphisms in Europeans and spontaneous pregnancy loss

Absence of BRAF V600E mutation in a cohort of 402 patients with various chronic and acute myeloid neoplasms

No association between the STAT5b rs6503691 (C>T) SNP and myeloproliferative neoplasms

Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report

Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

CALR versus JAK2 mutated essential thrombocythaemia - a report on 141 patients

HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania

CALR versus JAK2 mutated essential thrombocythaemia – a report on 141 patients

CALR versus JAK 2 mutated essential thrombocythaemia – a report on 141 patients

No association between the STAT 5b rs6503691 (C>T) SNP and myeloproliferative neoplasms

The G allele of the rs10974944 SNP, part of 46/1 haplotype, is strongly associated with V617F-positive myeloproliferative neoplasms

Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

The C677T Variant in the Methylenetetrahydrofolate Reductase Gene and Idiopathic Spontaneous Abortion in a Romanian Population Group

Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

Molecular basis and therapeutic targets in prostate cancer: A comprehensive review

Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array

The Impact of Chromosomal Mosaicisms on Prenatal Diagnosis and Genetic Counseling—A Narrative Review

Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive Review

A comprehensive review on the molecular basis and therapeutic targets in prostate cancer

Challenging diagnoses of tetraploidy/diploidy and trisomy 12: utility of first-tier prenatal testing methods

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