C. Kattamis

发表

Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods.

M. Tzetis, E. Kanavakis, J. Traeger-Synodinos, 1997, Molecular human reproduction.

Testicular damage in children and adolescents treated for malignancy: a short review

V. De Sanctis, A. Soliman, C. Kattamis, 2018, Acta bio-medica : Atenei Parmensis.

Long-Term Follow-up of β-Transfusion-Dependent Thalassemia (TDT) Normoglycemic Patients with Reduced Insulin Secretion to Oral Glucose Tolerance Test (OGTT): A Pilot Study

V. De Sanctis, A. Soliman, C. Kattamis, 2021, Mediterranean journal of hematology and infectious diseases.

Molecular Studies of β-Thalassemia Heterozygotes with Raised Hb F Levels

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000 .

Quantification of liver iron overload by T2 quantitative magnetic resonance imaging in thalassemia: impact of chronic hepatitis C on measurements.

A. Gouliamos, L. Nakopoulou, O. Papakonstantinou, 1999, Journal of pediatric hematology/oncology.

Haemoglobin Bart's hydrops syndrome in Greece.

J. Clegg, D. Weatherall, D. Higgs, 1980, British medical journal.

Longitudinal Study of Survival and Causes of Death in Patients with Thalassemia Major in Greece

E. Kanavakis, C. Kattamis, V. Ladis, 2005, Annals of the New York Academy of Sciences.

LACTOSE INTOLERANCE IN GREEKS

C. Kattamis, K. Anastassea-Vlachou, N. Matsaniotis, 1973 .

Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.

M. Tzetis, E. Kanavakis, C. Kattamis, 1998, Molecular human reproduction.

Glucose Metabolism and Insulin Response to Oral Glucose Tolerance Test (OGTT) in Prepubertal Patients with Transfusion-Dependent β-thalassemia (TDT): A Long-Term Retrospective Analysis

V. De Sanctis, A. Soliman, C. Kattamis, 2021, Mediterranean journal of hematology and infectious diseases.

Review and Recommendations on Management of Adult Female Thalassemia Patients with Hypogonadism based on Literature Review and Experience of ICET-A Network Specialists

V. De Sanctis, A. Soliman, S. A. Al Jaouni, 2016, Mediterranean journal of hematology and infectious diseases.

A high incidence of mutations in exon 6 of the low‐density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutation

S. Humphries, I. Day, E. Kanavakis, 1997 .

Diabetes and Glucose Metabolism in Thalassemia Major: An Update

V. De Sanctis, A. Soliman, A. Pepe, 2016, Expert review of hematology.

Marital status and paternity in patients with Transfusion-Dependent Thalassemia (TDT) and Non Transfusion-Dependent Thalassemia (NTDT): an ICET - A survey in different countries

V. De Sanctis, A. Soliman, M. Karimi, 2019, Acta bio-medica : Atenei Parmensis.

An ICET- A survey on hypoparathyroidism in patients with thalassaemia major and intermedia: a preliminary report

V. De Sanctis, S. A. Al Jaouni, M. Karimi, 2018, Acta bio-medica : Atenei Parmensis.

Clinical and Biochemical Data of Adult Thalassemia Major patients (TM) with Multiple Endocrine Complications (MEC) versus TM Patients with Normal Endocrine Functions: A long-term Retrospective Study (40 years) in a Tertiary Care Center in Italy

V. De Sanctis, A. Soliman, C. Kattamis, 2016, Mediterranean journal of hematology and infectious diseases.

A study of isolated hyperglycemia (blood glucose ≥155 mg/dL) at 1-hour of oral glucose tolerance test (OGTT) in patients with β-transfusion dependent thalassemia (β-TDT) followed for 12 years

V. De Sanctis, A. Soliman, C. Kattamis, 2021, Acta bio-medica : Atenei Parmensis.

Insulin-like Growth Factor-1 (IGF-1): Demographic, Clinical and Laboratory Data in 120 Consecutive Adult Patients with Thalassaemia Major

V. De Sanctis, A. Soliman, M. Karimi, 2014, Mediterranean journal of hematology and infectious diseases.

Bone density study at the distal radius, using pQCT analysis, in Greek thalassemic patients.

I. Papassotiriou, E. Papadopoulos, C. Kattamis, 2004, Pediatric endocrinology reviews : PER.

The different patterns of insulin response during oral glucose tolerance test (OGTT) in transfused young patients with β-thalassemia

N. Iacovidou, C. Kattamis, V. Ladis, 2021, Acta bio-medica : Atenei Parmensis.

OXIDATIVE STRESS DISTURBANCES IN ERYTHROCYTES OF ß-THALASSEMIA

C. Kattamis, A. Kattamis, 2001 .

Bone disease in β thalassemia patients: past, present and future perspectives.

V. De Sanctis, A. Soliman, C. Kattamis, 2017, Metabolism: clinical and experimental.

The Corfu δβ thalassaemia mutation in Greece: haematological phenotype and prevalence

M. Tzetis, E. Kanavakis, J. Traeger-Synodinos, 1991 .

A Novel Deletion in the β‐Globin Gene Complex

D. Weatherall, E. Kanavakis, S. Thein, 1985, Annals of the New York Academy of Sciences.

Molecular, haematological and clinical studies of the −101 C → T substitution of the β‐globin gene promoter in 25 β‐thalassaemia intermedia patients and 45 heterozygotes

J. Traeger-Synodinos, M. Tzetis, E. Kanavakis, 1999, British journal of haematology.

Pancreatic changes affecting glucose homeostasis in transfusion dependent β-thalassemia (TDT): a short review

V. De Sanctis, A. Soliman, C. Kattamis, 2021, Acta bio-medica : Atenei Parmensis.

Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000, British journal of haematology.

Red Cell Alloantibodies in Patients with Thalassemia

J. Peristeri, C. Kattamis, A. Hatziliami, 1990, Vox sanguinis.

The triplicated α‐globin gene locus in β‐thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies

J. Traeger-Synodinos, E. Kanavakis, J. Traeger-Synodinos, 1996 .

Dr. Messaritakis and co-workers comment

N. Matsaniotis, C. Kattamis, J. Messaritakis, 1976 .

Current treatment of hypoparathyroidism: theory versus reality waiting guidelines for children and adolescents

V. De Sanctis, A. Soliman, C. Kattamis, 2018, Acta bio-medica : Atenei Parmensis.

Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation.

M. Tzetis, E. Kanavakis, S. Doudounakis, 1995, Journal of medical genetics.

Three inherited red-cell abnormalities in a district of Greece. Thalassaemia, sickling, and glucose-6-phosphate-dehydrogenase deficiency.

G. Stamatoyannopoulos, C. Kattamis, P. Fessas, 1963, Lancet.

Clinical Response and Adverse Events in Young Patients with Sickle Cell Disease Treated with Hydroxyurea

E. Kanavakis, A. Kattamis, C. Kattamis, 2004, Pediatric hematology and oncology.

The clinical phenotype of β and δβ thalassemias in Greece

E. Kanavakis, C. Kattamis, V. Ladis, 1982, European Journal of Pediatrics.

Hypogonadism in male thalassemia major patients: pathophysiology, diagnosis and treatment

V. De Sanctis, A. Soliman, C. Kattamis, 2018, Acta bio-medica : Atenei Parmensis.

Rare beta-thalassemia alleles in the Greek and Greek Cypriot populations.

E. Kanavakis, J. Traeger-Synodinos, C. Vrettou, 1998, Hemoglobin.

A new δ chain variant hemoglobin A2-Corfu or α2δ2 116 Arg→Cys (G18), detected by δ-globin gene analysis in a Greek family

E. Kanavakis, G. Loudianos, M. Pirastu, 1991, Human Genetics.

Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia

V. De Sanctis, A. Soliman, M. Karimi, 2017, Expert review of hematology.

A multi-level intervention approach for care of HIV-positive haemophiliac and thalassaemic patients and their families.

J. Tsiantis, C. Kattamis, S. Aroni, 1990, AIDS care.

Two novel polyadenylation mutations leading to β+‐thalassaemia

C. Kattamis, T. Huisman, E. George, 1990 .

Characterization of Three Types of β0-Thaussemia Resulting from a Partial Deletion of the β-Globin Gene

T. Huisman, C. Kattamis, J. H. Gonzalez-Redondo, 1989 .

Preliminary mutation analysis in the phenylanaline hydroxylase gene in Greek PKU and HPA patients

E. Kanavakis, J. Traeger-Synodinos, C. Kattamis, 1994, Human Genetics.

Evolution of combined impaired fasting glucose and impaired glucose tolerance in β-thalassemia major: Results in 58 patients with a mean 7.7- year follow-up

V. De Sanctis, A. Soliman, C. Kattamis, 2022, Acta bio-medica : Atenei Parmensis.

The use of oral glucose-lowering agents (GLAs) in β-thalassemia patients with diabetes: Preliminary data from a retrospective study of ICET-A Network

T. Zarei, V. De Sanctis, A. Soliman, 2022, Acta bio-medica : Atenei Parmensis.

Regulation of Glucose Disturbances with Glibenclamide in Patients with Thalassemia

C. Kattamis, H. Berdousi, Fani Palamidou, 1998, Annals of the New York Academy of Sciences.

Iron chelation treatment with combined therapy with deferiprone and deferioxamine: a 12-month trial.

E. Alexopoulou, N. Kelekis, A. Kattamis, 2006, Blood cells, molecules & diseases.

Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.

N. Matsaniotis, C. Kattamis, A. Metaxotou-Mavromati, 1972, Journal of medical genetics.

Myxedema coma in children and adolescents: A rare endocrine emergency - Personal experience and review of literature

V. De Sanctis, A. Soliman, C. Kattamis, 2021, Acta bio-medica : Atenei Parmensis.

Thyroid Disorders in Homozygous β-Thalassemia: Current Knowledge, Emerging Issues and Open Problems

V. De Sanctis, A. Soliman, D. Canatan, 2019, Mediterranean journal of hematology and infectious diseases.

Evolution of glucose-insulin homeostasis in children with β- thalassemia major (β -TM): A twenty-year retrospective ICET- A observational analysis from early childhood to young adulthood

V. De Sanctis, A. Soliman, M. Karimi, 2022, Acta bio-medica : Atenei Parmensis.

ERYTHROCYTE ACID PHOSPHOMONOESTERASE IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE-DEFICIENT GREEKS

C. Kattamis, L. Zannos-Mariolea, C. Choremis, 1964 .

Screening for glucose dysregulation in β-thalassemia major (β-TM): An update of current evidences and personal experience

V. De Sanctis, A. Soliman, M. Karimi, 2022, Acta bio-medica : Atenei Parmensis.

Combined therapy with desferrioxamine and deferiprone in thalassemic patients: effect on urinary iron excretion.

I. Papassotiriou, A. Kattamis, C. Kattamis, 2003, Haematologica.

Beta-thalassaemia, G-6-PD deficiency, and atypical cholinesterase in Cyprus.

N. Matsaniotis, C. Kattamis, S. Haidas, 1972, British medical journal.

Glucose-6-phosphate dehydrogenase deficiency in Greece.

C. Kattamis, L. Zannos-Mariolea, 1961, Blood.

The Corfu deltabeta thalassemia deletion disrupts gamma-globin gene silencing and reveals post-transcriptional regulation of HbF expression.

Cameron S. Osborne, P. Fraser, C. Osborne, 2005, Blood.

Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines

M. Angastiniotis, V. De Sanctis, A. Soliman, 2013, Indian journal of endocrinology and metabolism.

Diabetes following mumps in sibs.

N. Matsaniotis, C. Kattamis, J. Messaritakis, 1971, Archives of disease in childhood.

Effective detection of active HCV infection: HCV RNA carrier state in a context free of hepatitis symptoms.

C. Kattamis, S. Kostaridou, C. Arapinis, 1997, Clinica chimica acta; international journal of clinical chemistry.

General principles of good transition care: a short review of the literature

S. Bernasconi, M. Angastiniotis, A. Soliman, 2015 .

Management of thalassemias: growth and development, hormone substitution, vitamin supplementation, and vaccination.

C. Kattamis, A. Kattamis, 1995, Seminars in hematology.

Detection of human cytomegalovirus and epstein-barr-virus by the polymerase chain-reaction in patients with Beta-thalassemia.

D. Spandidos, M. Ergazaki, T. Liloglou, 1994, Oncology reports.

Current Issues and Options for Hormonal Contraception in Adolescents and Young Adult Women With Sickle Cell Disease: An Update for Health Care Professionals

V. De Sanctis, A. Soliman, D. Canatan, 2020, Mediterranean journal of hematology and infectious diseases.

Frequency of Atypical Pseudocholinesterase in British and Mediterranean Populations

C. Kattamis, H. Lehmann, L. Zannos-Mariolea, 1962, Nature.

The pancreas in β-thalassemia major: MR imaging features and correlation with iron stores and glucose disturbunces

N. Gourtsoyiannis, O. Papakonstantinou, T. Maris, 2007, European Radiology.

A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutation.

S. Humphries, I. Day, E. Kanavakis, 1997, Human mutation.

Oral glucose tolerance test: how to maximize its diagnostic value in children and adolescents

V. De Sanctis, A. Soliman, C. Kattamis, 2022, Acta bio-medica : Atenei Parmensis.

Generalized seborrhoeic dermatitis. Clinical and therapeutic data of 25 patients.

N. Matsaniotis, C. Kattamis, J. Messaritakis, 1975, Archives of disease in childhood.

Acquired Hypogonadotropic Hypogonadism (AHH) in Thalassaemia Major Patients: An Underdiagnosed Condition?

V. De Sanctis, A. Soliman, A. Pepe, 2016, Mediterranean journal of hematology and infectious diseases.

Frequency of α‐thalassemia in Greece

E. Kanavakis, S. Tzotzos, C. Kattamis, 1986 .

Endocrine profile of β-thalassemia major patients followed from childhood to advanced adulthood in a tertiary care center

V. De Sanctis, A. Soliman, C. Kattamis, 2016, Indian journal of endocrinology and metabolism.

Thalassemias, Abnormal Hemoglobins and Glucose‐6‐Phosphate Dehydrogenase Deficiency in the Arta Area of Greece: Diagnostic and Genetic Aspects of Complete Village Studies *

G. Stamatoyannopoulos, A. Motulsky, G. Fraser, 1964, Annals of the New York Academy of Sciences.

Glucose‐6‐phosphate dehydrogenase, colour vision and Xg blood groups in Greece: linkage and population data

G. Stamatoyannopoulos, G. Fraser, C. Kattamis, 1963, Annals of human genetics.

β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical Standpoint

M. Angastiniotis, V. De Sanctis, A. Soliman, 2017, Mediterranean journal of hematology and infectious diseases.

Effectiveness of one tube osmotic fragility screening in detecting beta-thalassaemia trait.

C. Kattamis, G. Efremov, S. Pootrakul, 1981, Journal of medical genetics.

Screening for Hemoglobinopathies (Thalassemias and Other Abnormal Hemoglobins)

C. Kattamis, 1980 .

The Clinical and Haematological Findings in Children Inheriting Two Types of Thalassaemia: High‐A2 Type β‐Thalassaemia, and High‐F Type or δβ‐Thalassaemia

H. Lehmann, C. Kattamis, A. Metaxotou-Mavromati, 1973 .

The Heterogeneity of Normal Hb A2‐β Thalassaemia in Greece

D. Weatherall, C. Kattamis, J. Nash, 1979 .

G6PD deficiency and favism in the island of Rhodes (Greece).

C. Kattamis, A. Chaidas, S. Chaidas, 1969, Journal of medical genetics.

Glucose-6-phosphate Dehydrogenase Activity Levels in Enzyme-deficient Greek Individuals*

C. Kattamis, P. Paraschopoulou-Prevedouraki, L. Zannos-Mariolea, 1963, British medical journal.

Impairment of cardiac function in a successful full-term pregnancy in a homozygous beta-thalassemia major: does chelation have a positive role?

M. Tsironi, S. Deftereos, C. Kattamis, 2005, European journal of obstetrics, gynecology, and reproductive biology.

Urinary excretion of acid muco-polysaccharide in sibs with Morquio's syndrome and Reilly's granules in leucocytes.

H. Lehmann, N. Matsaniotis, C. Kattamis, 1967, Archives of disease in childhood.

Insulin-like growth factor -1 (IGF-1) and glucose dysregulation in young adult patients with β-thalassemia major: causality or potential link?

V. De Sanctis, A. Soliman, C. Kattamis, 2022, Acta bio-medica : Atenei Parmensis.

Clinical characteristics, biochemical parameters and insulin response to oral glucose tolerance test (OGTT) in 25 transfusion dependent β-thalassemia (TDT) patients recently diagnosed with diabetes mellitus (DM)

V. De Sanctis, A. Soliman, M. Karimi, 2022, Acta bio-medica : Atenei Parmensis.

Prevalence of glucose dysregulation (GD) in patients with β-thalassemias in different countries: A preliminary ICET-A survey

V. De Sanctis, A. Soliman, S. A. Al Jaouni, 2021, Acta bio-medica : Atenei Parmensis.

The ICET-A Recommendations for the Diagnosis and Management of Disturbances of Glucose Homeostasis in Thalassemia Major Patients

M. Angastiniotis, V. De Sanctis, A. Soliman, 2016, Mediterranean journal of hematology and infectious diseases.

International network on endocrine complications in thalassaemia (I-CET): an opportunity to grow.

M. Angastiniotis, A. Eleftheriou, V. De Sanctis, 2012, Georgian medical news.

Evolution of glucose intolerance and diabetes in transfused patients with thalassemia.

C. Kattamis, V. Ladis, I. Kaloumenou, 2004, Pediatric endocrinology reviews : PER.

Growth and management of short stature in thalassaemia major.

C. Kattamis, H. Berdousi, A. Papatheodorou, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Gonadotropin replacement in male thalassemia major patients with arrested puberty and acquired hypogonadotropic hypogonadism (AAH): preliminary results and potential factors affecting induction of spermatogenesis

S. Maio, A. Soliman, D. Canatan, 2018, Endocrine.

Does Insulin Like Growth Factor-1 (IGF-1) Deficiency Have a “Protective” Role in the Development of Diabetic Retinopathy in Thalassamia Major Patients?

V. De Sanctis, A. Soliman, A. Pepe, 2015, Mediterranean journal of hematology and infectious diseases.

Favism Clinical and Biochemical Data

C. Kattamis, S. Chaidas, M. Kyriazakou, 2006 .

Prevalence of Au-Ag and Au-Ab in transfused children with thalassaemia in Greece

N. Matsaniotis, C. Kattamis, D. Demetriou, 1974, Archives of disease in childhood.

Coronavirus Disease 2019 (COVID-19) in adolescents: An update on current clinical and diagnostic characteristics

V. De Sanctis, A. Soliman, C. Kattamis, 2020, Acta bio-medica : Atenei Parmensis.

DIFFERENTIATION BETWEEN NEONATAL HEPATITIS AND BILIARY ATRESIA BY MEASURING SERUM-ALPHA-FETOPROTEIN

C. Kattamis, N. Matsaniotis, S. Laskari, 1974 .

Neonatal hepatitis associated with Australia antigen (Au-1).

N. Matsaniotis, C. Kattamis, D. Demetriou, 1973, Archives of disease in childhood.

Prevalence of yersinia plasmid-encoded outer protein (Yop) class-specific antibodies in multitransfused Greek patients with thalassemic syndromes.

C. Kattamis, S. Chatzipanagiotou, H. Berdousi, 1999, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

The triplicated α gene locus and β thalassaemia

W. Wood, J. Wainscoat, C. Kattamis, 1983 .

The triplicated alpha gene locus and beta thalassaemia.

E. Kanavakis, W. Wood, J. Wainscoat, 1983, British journal of haematology.

Occurrence of Gγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia

J. Clegg, D. Weatherall, C. Kattamis, 1979 .

Abdominal ultrasonographic findings in patients with sickle-cell anaemia and thalassaemia intermedia

C. Kattamis, A. Kattamis, T. Georgakopoulou, 2003, Pediatric Radiology.

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks.

F. Collins, G. Stamatoyannopoulos, M. Bender, 1986, Blood.

Characterization of nondeletion α‐thalassemia mutations in the Greek population

M. Tzetis, E. Kanavakis, J. Traeger-Synodinos, 1993 .

A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia

D. Higgs, J. Traeger-Synodinos, E. Kanavakis, 1993 .

CORRELATION OF CLINICAL PHENOTYPE TO GENOTYPE IN HAEMOGLOBIN H DISEASE

E. Kanavakis, S. Tzotzos, C. Kattamis, 1988, The Lancet.

The molecular basis of HbH disease in Greece

E. Kanavakis, S. Tzotzos, C. Kattamis, 1986, British journal of haematology.

reveals post-transcriptional regulation of HbF expression -globin gene silencing and γ thalassemia deletion disrupts β δ

Cameron S. Osborne, P. Fraser, C. Osborne, 2013 .

The Corfu δβ thalassemia deletion disrupts γ-globin gene silencing and reveals post-transcriptional regulation of HbF expression Running title: Corfu δβ thalassemia and β-globin regulation

Cameron S. Osborne, P. Fraser, C. Osborne, 2005 .

Sustained response to interferon alpha-2a in thalassemic patients with chronic hepatitis C. A prospective 8-year follow-up study.

L. Nakopoulou, G. Daikos, V. Syriopoulou, 2005, Haematologica.

The hemolytic process of viral hepatitis in children with normal or deficient glucose-6-phosphate dehydrogenase activity.

C. Kattamis, F. Tjortjatou, Ch. Kattamis, 1970, The Journal of pediatrics.

IMMUNE RESPONSES TO HEPATITIS B VACCINE

P. Coursaget, A. Goudeau, C. Kattamis, 1981, The Lancet.

Australia antigen and neonatal hepatitis syndrome.

N. Matsaniotis, C. Kattamis, D. Demetrios, 1974, Pediatrics.

Serum ferritin in beta-thalassaemia intermedia.

N. Matsaniotis, C. Kattamis, E. Lagona, 1980, Lancet.

Molecular characterization of β‐thalassaemia in 174 Greek patients with thalassaemia major

A. Kutlar, C. Kattamis, T. Huisman, 1990, British journal of haematology.

Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in Greece.

M. Tzetis, E. Kanavakis, J. Traeger-Synodinos, 1995, Pediatric hematology and oncology.

The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.

M. Tzetis, E. Kanavakis, J. Traeger-Synodinos, 1994, Hematologic pathology.

A Comparison of the Homozygous States for Gγ and GγAγδβ Thalassaemia

J. Clegg, D. Weatherall, J. White, 1979 .

A comparison of the homozygous states for G gamma and G gamma A gamma delta beta thalassaemia.

J. Clegg, D. Weatherall, W. Wood, 1979, British journal of haematology.

Prevalence of β0 and β+ Thalassemia Genes in Greek Children with Homozygous β-Thalassemia

C. Kattamis, V. Ladis, A. Metaxotou-Mavromati, 1978 .

Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000, Hemoglobin.

Growth of Children with Thalassaemia

N. Matsaniotis, C. Kattamis, S. Haidas, 1970, Archives of disease in childhood.

Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study

Y. Oymak, T. Zarei, V. De Sanctis, 2020, Mediterranean journal of hematology and infectious diseases.

The ICET-A Survey on Current Criteria Used by Clinicians for the Assessment of Central Adrenal Insufficiency in Thalassemia: Analysis of Results and Recommendations

M. Di Maio, V. De Sanctis, A. Soliman, 2016, Mediterranean journal of hematology and infectious diseases.

Glucose Homeostasis and Assessment of β-Cell Function by 3-hour Oral Glucose Tolerance (OGTT) in Patients with β-Thalassemia Major with Serum Ferritin below 1,000 ng/dL: Results from a Single ICET-A Centre

V. De Sanctis, A. Soliman, C. Kattamis, 2023, Mediterranean journal of hematology and infectious diseases.

An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 1998, Hemoglobin.

Genetic and molecular diversity in nondeletion Hb H disease.

J. Clegg, D. Weatherall, D. Higgs, 1981, Proceedings of the National Academy of Sciences of the United States of America.

DUPLICATION OF ALPHA-THALASSÆMIA GENE IN THREE GREEK FAMILIES WITH HÆMOGLOBIN H DISEASE

H. Lehmann, C. Kattamis, 1970 .

Duplication of alpha-thalassaemia gene in three Greek families with haemoglobin H disease.

H. Lehmann, C. Kattamis, 1970, Lancet.

Tissue oxygenation in patients with hemoglobinopathy H.

I. Papassotiriou, E. Kanavakis, C. Kattamis, 1997, Pediatric hematology and oncology.

Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemia.

E. Kanavakis, J. Traeger-Synodinos, L. Bernini, 1999, Hemoglobin.

Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA].

M. Fichera, J. Traeger-Synodinos, E. Kanavakis, 2001, Haematologica.

The juvenile fibromyalgia syndrome (JFMS): a poorly defined disorder

V. De Sanctis, A. Soliman, C. Kattamis, 2019, Acta bio-medica : Atenei Parmensis.

Prevalence, attitude and practice of self-medication among adolescents and the paradigm of dysmenorrhea self-care management in different countries

V. De Sanctis, A. Soliman, C. Kattamis, 2020, Acta bio-medica : Atenei Parmensis.

Non-invasive myocardial iron assessment in thalassaemic patients: T2 relaxometry and magnetization transfer ratio measurements

Nickolas Papanikolaou, A. Ghiatas, A. Kattamis, 2000 .

Relapse of herpes simplex encephalitis after acyclovir therapy

N. Iacovidou, P. Nicolaidou, C. Kattamis, 1993, European Journal of Pediatrics.

The Impact of Neocyte Transfusion in the Management of Thalassaemia

I. Papassotiriou, C. Kattamis, E. Premetis, 1996, Vox sanguinis.

Assessment of liver iron overload by T2-quantitative magnetic resonance imaging: correlation of T2-QMRI measurements with serum ferritin concentration and histologic grading of siderosis.

T G Maris, L. Vlahos, A. Gouliamos, 1995, Magnetic resonance imaging.

Correlation of in vitro enhancement of erythropoiesis and clinical response to steroids in Diamond-Blackfan anaemia.

M. Kalmanti, C. Kattamis, H. Dimitriou, 1993, Haematologia.

Relation of chelation regimes to cardiac mortality and morbidity in patients with thalassaemia major: an observational study from a large Greek Unit

P. Moraitis, C. Kattamis, G. Chouliaras, 2010, European journal of haematology.

A Concise Review on the Frequency, Major Risk Factors and Surveillance of Hepatocellular Carcinoma (HCC) in β-Thalassemias: Past, Present and Future Perspectives and the ICET-A Experience

V. De Sanctis, A. Soliman, S. A. Al Jaouni, 2020, Mediterranean journal of hematology and infectious diseases.

Liver Iron Concentration and Liver Impairment in Relation to Serum IGF-1 Levels in Thalassaemia Major Patients: A Retrospective Study

V. De Sanctis, A. Soliman, C. Kattamis, 2015, Mediterranean journal of hematology and infectious diseases.

The genetical interpretation of haemoglobin H disease.

H. Lehmann, C. Kattamis, 1970, Human heredity.

Infantile Pyknocytosis and Glucose‐6‐Phosphate Dehydrogenase Deficiency *

C. Kattamis, L. Zannos-Mariolea, Leda Zannos—Mariolea, 1962, British journal of haematology.

Hepatitis G virus or hepatitis GB virus type C infection in thalassemic patients

C. Kattamis, S. Hadziyannis, E. Spanou, 1999, Transfusion.

Growth and Development in Children with Thalassaemia Major

A. Kattamis, C. Kattamis, T. Liakopoulou, 1990, Acta paediatrica Scandinavica. Supplement.

The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.

E. Kanavakis, J. Traeger-Synodinos, C. Vrettou, 1996, British journal of haematology.

Glucose‐6‐Phosphate Dehydrogenase Deficiency in Female Heterozygoses and the X‐Inactivation Hypothesis

C. Kattamis, 1967, Acta paediatrica Scandinavica.

Brucellosis in two thalassaemic patients infected by blood transfusions from the same donor.

D. Petropoulou, C. Kattamis, J. Economidou, 1976, Acta haematologica.

Acute Glomerulonephritis I. Radiological changes of the lungs (Incidence, types and relation to oedema, hypertension and uremia)

C. Kattamis, XENOPHON NICOLAIDES, 1967, Acta paediatrica Scandinavica.

Globin gene mapping in normal Hb A2 types of β‐thalassaemia

D. Weatherall, E. Kanavakis, C. Kattamis, 1982, British journal of haematology.

Characterization of nondeletion alpha-thalassemia mutations in the Greek population.

M. Tzetis, E. Kanavakis, J. Traeger-Synodinos, 1993, American journal of hematology.

FALSE-POSITIVE HTLV-III ANTIBODY TESTS IN MULTITRANSFUSED PATIENTS WITH THALASSAEMIA

C. Kattamis, A. Tzivaras, V. Michail-Merianou, 1986, The Lancet.

Tissue immunodetection of c100 hepatitis C virus antigen in major thalassemic patients.

A. Lazaris, P. Davaris, L. Nakopoulou, 1999, Hepato-Gastroenterology.

The pancreas in beta-thalassemia major: MR imaging features and correlation with iron stores and glucose disturbances.

N. Gourtsoyiannis, O. Papakonstantinou, T. Maris, 2007, European radiology.

Retrospective observational studies: Lights and shadows for medical writers

V. De Sanctis, A. Soliman, C. Kattamis, 2022, Acta bio-medica : Atenei Parmensis.

Some clinical and biochemical aspects of favism in childhood.

C. Kattamis, 1969, Annales des Societes belges de medecine tropicale, de parasitologie, et de mycologie.

Viral hepatitis in G.-6-P.D. deficiency.

C. Kattamis, C. Choremis, M. Kyriazakou, 1966, Lancet.

FAVISM: EPIDEMIOLOGICAL AND CLINICAL ASPECTS

C. Kattamis, 1986 .

SCREENING FOR BETA-THALASSAEMIAS

C. Kattamis, A. Metaxotou-Mavromati, N. Matsaniotis, 1981, The Lancet.

Glucose-6-Phosphate Dehydro-genase Deficiency in Greece.

C. Kattamis, L. Zannos-Mariolea, 1961 .

Heart failure in beta thalassemia: a 5-year follow-up study.

D. Tsiapras, D. Kremastinos, C. Kattamis, 2001, The American journal of medicine.

Glucose disturbances and regulation with glibenclamide in thalassemia.

C. Kattamis, H. Berdousi, V. Ladis, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Deferasirox (Exjade®) in Pediatric Patients with β-Thalassemia: Update of 4.7-Year Efficacy and Safety from Extension Studies

R. Galanello, A. Piga, G. Forni, 2008 .

Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study

T. Zarei, V. De Sanctis, A. Soliman, 2019, Endocrine.

A Comprehensive Update of ICET-A Network on COVID-19 in Thalassemias: What We Know and Where We Stand

Y. Oymak, T. Zarei, V. De Sanctis, 2020, Acta bio-medica : Atenei Parmensis.

Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.

M. Tzetis, E. Kanavakis, L. Stefanis, 1994, Pediatric hematology and oncology.

Haplotype and mutation analysis in Greek patients with Wilson disease

M. Tzetis, E. Kanavakis, A. Angius, 1998, European Journal of Human Genetics.

Deferasirox (Exjade®, ICL670) Demonstrates Iron Chelating Efficacy Related to Transfusional Iron Intake in Pediatric Patients.

J. Ford, T. Klingebiel, Y. Kilinç, 2005 .

Activity of ribonuclease H in cells of chronic B‐lymphocytic leukaemia: correlation with clinical stage

C. Kattamis, E. Kamper, G. Pangalis, 1988, British journal of haematology.

1342C mutation in Gaucher's disease

E. Beutler, J. Sipe, C. Kattamis, 1995, The Lancet.

Bullous emphysema in childhood tuberculosis.

C. Kattamis, N. Matsaniotis, M. Kyriazakou, 1967, The Journal of pediatrics.

Oxidative stress disturbances in erythrocytes of beta-thalassemia.

C. Kattamis, A. Kattamis, 2001, Pediatric Hematology & Oncology.

The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H

E. Kanavakis, J. Traeger-Synodinos, C. Vrettou, 1996 .

Non-invasive myocardial iron assessment in thalassaemic patients. T2 relaxometry and magnetization transfer ratio measurements.

Nickolas Papanikolaou, A. Ghiatas, A. Kattamis, 2000, Acta radiologica.

A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemia.

D. Higgs, E. Kanavakis, S. Thein, 1993, British journal of haematology.

ORAL DESFERRIOXAMINE IN YOUNG PATIENTS WITH THALASSAEMIA

C. Kattamis, J. Fitsialos, Cleo Sinopoulou, 1981, The Lancet.

Study of bone density by pQCT analysis in healthy adults and patients with B-thalassemia major and intermedia.

A. Galanos, P. Raptou, C. Kattamis, 2008, Pediatric endocrinology reviews : PER.

Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations

M. Tzetis, E. Kanavakis, S. Doudounakis, 1996, Human Genetics.

Assessment of glucose homeostasis in young adult female β-thalassemia major patients (β-TM) with acquired hypogonadotropic hypogonadism (AHH) never treated with sex steroids compared to eugonadal β-TM patients with spontaneous menstrual cycles

V. De Sanctis, A. Soliman, C. Kattamis, 2023, Acta bio-medica : Atenei Parmensis.

Longitudinal study of ICET-A on glucose tolerance, insulin sensitivity and β-cell secretion in eleven β-thalassemia major patients with mild iron overload

V. De Sanctis, A. Soliman, C. Kattamis, 2023, Acta bio-medica : Atenei Parmensis.

Two novel polyadenylation mutations leading to beta(+)-thalassemia.

T. Huisman, C. Kattamis, G. Efremov, 1990, British journal of haematology.

Favism in breast-fed infants.

C. Kattamis, 1971, Archives of disease in childhood.

Heterozygosity of the Complex Corfu δ0β+ Thalassemic Allele (HBD Deletion and HBB:c.92+5G>A) Revisited

J. Traeger-Synodinos, C. Vrettou, C. Sofocleous, 2022, Biology.

Adult‐onset beta‐thalassaemia intermedia caused by a 5‐Mb somatic clonal segmental deletion in haemopoietic stem cells involving the β‐globin locus

C. Ruivenkamp, E. Kanavakis, J. Traeger-Synodinos, 2019, British journal of haematology.

Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation

M. Tzetis, E. Kanavakis, S. Doudounakis, 1995, Human Genetics.

Jaundice and bilirubin levels in Greek children with favism.

C. Kattamis, V. Ioannidou, K. Karambula, 1976, Archives of disease in childhood.

The interaction of alpha zero thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H.

E. Kanavakis, J. Traeger-Synodinos, C. Vrettou, 1996, British Journal of Haematology.

Gaucher disease: four families with previously undescribed mutations.

L. Elsas, D. Balicki, R. Gitzelmann, 1996, Proceedings of the Association of American Physicians.

Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients.

M. Tzetis, E. Kanavakis, S. Doudounakis, 1995, Molecular and cellular probes.

Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia

V. De Sanctis, A. Soliman, M. Karimi, 2017, Expert review of hematology.

Hypomenorrhea in Adolescents and Youths: Normal Variant or Menstrual Disorder ? Revision of Literature and Personal Experience

V. De Sanctis, A. Soliman, C. Kattamis, 2022, Acta bio-medica : Atenei Parmensis.

Unilateral breast enlargement in males during adolescence (10-19 years): review of current literature and personal experience

V. De Sanctis, A. Soliman, C. Kattamis, 2023, Acta bio-medica : Atenei Parmensis.

Urinary excretion of acid muco-polysaccharide in sibs with Morquio's syndrome and Reilly's granules in leucocytes.

H. Lehmann, N. Matsaniotis, C. Kattamis, 1967, Archives of disease in childhood.

Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probands

S. Humphries, I. Day, E. Kanavakis, 1998, Human Genetics.

Aldrich's syndrome (thrombocytopenia, eczema, and recurrent infections). Report of a case.

E. Kanavakis, C. Kattamis, C. Cassimos, 1960, American journal of diseases of children.

An ICET-A survey on occult and emerging endocrine complications in patients with β-thalassemia major: Conclusions and recommendations

V. De Sanctis, A. Soliman, S. A. Al Jaouni, 2019, Acta bio-medica : Atenei Parmensis.