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Maternal diabetes and the role of neonatal reticulocyte hemoglobin content as a biomarker of iron status in the perinatal period

Frontiers in endocrinology (Lausanne), 2022-11, Vol.13, p.1011897-1011897

2022

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TACI Mutations in Primary Antibody Deficiencies: A Nationwide Study in Greece

Medicina (Kaunas, Lithuania), 2021-08, Vol.57 (8), p.827

2021

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A case of palisaded neutrophilic granulomatous dermatitis with subsequent development of chronic myelomonocytic leukemia

Clinical case reports, 2019-04, Vol.7 (4), p.695-698

2019

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A retrospective study of azacitidine treatment in patients with intermediate-2 or high risk myelodysplastic syndromes in a real-world clinical setting in Greece

International journal of hematology, 2017-02, Vol.105 (2), p.184-195

2017

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Women's Issues in Antiphospholipid Syndrome

The Israel Medical Association journal, 2016-09, Vol.18 (9), p.524-529

2016

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Neonatal haemostatic parameters in correlation to gestational age and birth weight

International journal of laboratory hematology, 2022-10, Vol.44 (5), p.952-958

2022

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A case of successful management with splenectomy of intractable ascites due to congenital dyserythropoietic anemia type II-induced cirrhosis

World journal of gastroenterology : WJG, 2006-02, Vol.12 (5), p.818

2006

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Reply to: “SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting”

Journal of hepatology, 2013-08, Vol.59 (2), p.397-397

2013

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Isolated Splenic Mycobacterial Disease: A Cause of Persistent Fever in a Hairy Cell Leukemia Patient

Case reports in gastroenterology, 2010-09, Vol.4 (3), p.330-334

2010

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Pulmonary co‐infections by Pneumocystis jirovecii and Aspergillus fumigatus in non‐HIV patients: A report of two cases and literature review

Mycoses, 2017-10, Vol.60 (10), p.626-633

2017

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Lack of survival improvement with novel anti-myeloma agents for patients with multiple myeloma and central nervous system involvement: the Greek Myeloma Study Group experience

Annals of hematology, 2015-12, Vol.94 (12), p.2033-2042

2015

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Patients with Myelodysplastic Syndromes, Other Than Del(5)q Syndrome, Exhibiting Del(5)q Alone or Associated with One Additional Chromosomal Abnormality Have Comparable Probability and Duration of Response to Lenalidomide, with Patients Classified As Del(5)q Syndrome

Blood, 2017-12, Vol.130, p.1696-1696

2017

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Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia

Journal of pediatric hematology/oncology, 2014-07, Vol.36 (5), p.e304-e306

2014

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SLC40A1- R178G mutation and ferroportin disease

Journal of hepatology, 2011-09, Vol.55 (3), p.730-731

2011

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Correction to: Real-world data on Len/Dex combination at second-line therapy of multiple myeloma: treatment at biochemical relapse is a significant prognostic factor for progression-free survival

Annals of hematology, 2018-09, Vol.97 (9), p.1747-1747

2018

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Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis

Journal of the neurological sciences, 2014-04, Vol.339 (1), p.220-222

2014

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Correlations of JAK2–V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders

Leukemia research, 2007-08, Vol.31 (8), p.1053-1062

2007

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Impact of Inherited Thrombophilia Factors On Thrombotic Risk in Patients with Newly Diagnosed BCR- Abl (-) Myeloproliferative Disorders; Finally a Role of MTHFR- C677T Polymorphism?

Blood, 2012-11, Vol.120 (21), p.5065-5065

2012

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Primary cutaneous follicle center lymphoma, diffuse type, with atypical clinical features

EJD. European journal of dermatology, 2014-03, Vol.24 (2), p.249-250

2014

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A Case of Infectious Mononucleosis Complicated by Severe Thrombocytopenia and Hyperuricemia

Open journal of blood diseases, 2016, Vol.6 (1), p.6-8

2016

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Corrigendum to: Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV [Blood Cells Mol. Dis. 40:3 (2008) 353–359]

Blood cells, molecules, & diseases, 2013-06, Vol.51 (1), p.69-69

2013

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Anatomical Distribution of First VTE Event and Risk of VTE Recurrence: Long Term Follow-up and Retrospective Analysis of 346 Patients. Experience From a Single Center

Blood, 2011-11, Vol.118 (21), p.1224-1224

2011

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Maternal diabetes and the role of neonatal reticulocyte hemoglobin content as a biomarker of iron status in the perinatal period

Real-world data on Len/Dex combination at second-line therapy of multiple myeloma: treatment at biochemical relapse is a significant prognostic factor for progression-free survival

TACI Mutations in Primary Antibody Deficiencies: A Nationwide Study in Greece

A case of palisaded neutrophilic granulomatous dermatitis with subsequent development of chronic myelomonocytic leukemia

A retrospective study of azacitidine treatment in patients with intermediate-2 or high risk myelodysplastic syndromes in a real-world clinical setting in Greece

Women's Issues in Antiphospholipid Syndrome

Neonatal haemostatic parameters in correlation to gestational age and birth weight

A case of successful management with splenectomy of intractable ascites due to congenital dyserythropoietic anemia type II-induced cirrhosis

Reply to: “SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting”

Plasmic and Plasic Αre Εxcellent Predictors of Severe ADAMTS13 Deficiency in Thrombotic Microangiopathy Patients without Secondary Causes

Isolated Splenic Mycobacterial Disease: A Cause of Persistent Fever in a Hairy Cell Leukemia Patient

Pulmonary co‐infections by Pneumocystis jirovecii and Aspergillus fumigatus in non‐HIV patients: A report of two cases and literature review

Lack of survival improvement with novel anti-myeloma agents for patients with multiple myeloma and central nervous system involvement: the Greek Myeloma Study Group experience

Patients with Myelodysplastic Syndromes, Other Than Del(5)q Syndrome, Exhibiting Del(5)q Alone or Associated with One Additional Chromosomal Abnormality Have Comparable Probability and Duration of Response to Lenalidomide, with Patients Classified As Del(5)q Syndrome

Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia

SLC40A1- R178G mutation and ferroportin disease

Correction to: Real-world data on Len/Dex combination at second-line therapy of multiple myeloma: treatment at biochemical relapse is a significant prognostic factor for progression-free survival

Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis

Correlations of JAK2–V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders

Impact of Inherited Thrombophilia Factors On Thrombotic Risk in Patients with Newly Diagnosed BCR- Abl (-) Myeloproliferative Disorders; Finally a Role of MTHFR- C677T Polymorphism?

Primary cutaneous follicle center lymphoma, diffuse type, with atypical clinical features

A Case of Infectious Mononucleosis Complicated by Severe Thrombocytopenia and Hyperuricemia

Corrigendum to: Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV [Blood Cells Mol. Dis. 40:3 (2008) 353–359]

Real-world data of thrombotic microangiopathy management: The key role of ADAMTS13 activity and complement testing

Anatomical Distribution of First VTE Event and Risk of VTE Recurrence: Long Term Follow-up and Retrospective Analysis of 346 Patients. Experience From a Single Center

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