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Congenital hypothyroidism: a case report of an Egyptian child with congenital heart disease, pelvic kidney and cavernous transformation of portal vein

The Egyptian journal of medical human genetics, 2023-12, Vol.24 (1), p.28

2023

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Ambulatory Duchenne muscular dystrophy children: cross-sectional correlation between function, quantitative muscle ultrasound and MRI

Acta myologica, 2022-03, Vol.41 (1), p.1-14

2022

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Striae distensae in adolescents: A mini review

Acta bio-medica : Atenei Parmensis, 2020-03, Vol.91 (1), p.176-181

Elsedfy, Heba

2020

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CLINICAL AND BIOCHEMICAL DATA OF ADULT THALASSEMIA MAJOR PATIENTS (TM) WITH MULTIPLE ENDOCRINE COMPLICATIONS (MEC) VERSUS TM PATIENTS WITH NORMAL ENDOCRINE FUNCTIONS: A RETROSPECTIVE LONG-TERM STUDY (40 YEARS) IN A TERTIARY CARE CENTER IN ITALY

Mediterranean journal of hematology and infectious diseases, 2016-04, Vol.8, p.2016022-e2016022

2016

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The Diagnostic Approach to Central Adrenocortical Insufficiency (CAI) in Thalassemia

Mediterranean journal of hematology and infectious diseases, 2016-05, Vol.8 (1), p.e2016026-e2016026

2016

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The experience of a tertiary unit on the clinical phenotype and management of hypogonadism in female adolescents and young adults with transfusion dependent thalassemia

Acta bio-medica : Atenei Parmensis, 2019-01, Vol.90 (1), p.158-167

2019

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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

Mediterranean journal of hematology and infectious diseases, 2016, Vol.8 (1), p.e2016022-e2016022

2016

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Serum α-klotho levels are not informative for the evaluation of growth hormone secretion in short children

Journal of pediatric endocrinology & metabolism : JPEM, 2017-10, Vol.30 (10), p.1055

2017

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Penile length and genital anomalies in Egyptian male newborns: epidemiology and influence of endocrine disruptors

Journal of Pediatric Endocrinology and Metabolism, 2013-05, Vol.26 (5), p.509-513

2013

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A clinical approach to benign breast lesions in female adolescents

Acta bio-medica de l'Ateneo Parmense, 2017-08, Vol.88 (2), p.214-221, Article 214

Elsedfy, Heba

2017

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Uterine development in patients with Turner syndrome: Relation to hormone replacement therapy and karyotype

Journal of Pediatric Endocrinology and Metabolism, 2012-06, Vol.25 (5), p.441-445

2012

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

Mediterranean journal of hematology and infectious diseases, 2016, Vol.8 (1), p.e2016058-e2016058

2016

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

Mediterranean journal of hematology and infectious diseases, 2016, Vol.8 (1), p.e2016001-e2016001

2016

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Pegvisomant-primed growth hormone (GH) stimulation test is useful in identifying true GH deficient children

Hormones (Athens, Greece), 2017-07, Vol.16 (3), p.291-296

2017

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Pegvisomant-primed growth hormone (GH) stimulation test is useful in identifying true GH deficient children

Hormones (Athens, Greece), 2017-07, Vol.13 (3), p.291-296

2017

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Effect of GnRH analogue on height potential in patients with severe growth hormone insensitivity syndrome treated with IGF-I

Journal of Pediatric Endocrinology and Metabolism, 2011-12, Vol.24 (11-12), p.983-988

2011

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Does Testosterone Replacement Therapy Promote an Augmented Risk of Thrombotic Events in Thalassemia Major Male Patients with Hypogonadism?

Indian journal of endocrinology and metabolism, 2017-07, Vol.21 (4), p.636-637

2017

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Current practice in treating adult female thalassemia major patients with hypogonadism: An International Network of Clinicians for Endocrinopathies in Thalassemia and Adolescence Medicine survey from Italy

Indian journal of endocrinology and metabolism, 2016-11, Vol.20 (6), p.880-881

2016

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Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre

Endocrine Connections, 2021-09, Vol.10 (9), p.1134-1146

2021

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Ovarian reserve and fertility parameters in post-pubertal females with congenital adrenal hyperplasia: a case-control study

Journal of pediatric endocrinology & metabolism : JPEM, 2024-04, Vol.37 (4), p.336

2024

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THE ICET-A SURVEY ON CURRENT CRITERIA USED BY CLINICIANS FOR THE ASSESSMENT OF CENTRAL ADRENAL INSUFFICIENCY IN THALASSEMIA: ANALYSIS OF RESULTS AND RECOMMENDATIONS

Mediterranean journal of hematology and infectious diseases, 2016-07, Vol.8 (1), p.e2016034-e2016034

De Sanctis, Vincenzo

2016

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Insulin resistance in obese pre-pubertal children: Relation to body composition

The Egyptian journal of medical human genetics, 2014-07, Vol.15 (3), p.249-255

2014

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The recommendation of the International Network of Clinicians for Endocrinopathies in Thalassemia and Adolescent Medicine for the assessment of growth hormone secretion in thalassemia

Indian journal of endocrinology and metabolism, 2015-03, Vol.19 (2), p.306-307

2015

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Congenital hypothyroidism: a case report of an Egyptian child with congenital heart disease, pelvic kidney and cavernous transformation of portal vein

Treatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

Ambulatory Duchenne muscular dystrophy children: cross-sectional correlation between function, quantitative muscle ultrasound and MRI

Striae distensae in adolescents: A mini review

CLINICAL AND BIOCHEMICAL DATA OF ADULT THALASSEMIA MAJOR PATIENTS (TM) WITH MULTIPLE ENDOCRINE COMPLICATIONS (MEC) VERSUS TM PATIENTS WITH NORMAL ENDOCRINE FUNCTIONS: A RETROSPECTIVE LONG-TERM STUDY (40 YEARS) IN A TERTIARY CARE CENTER IN ITALY

The Diagnostic Approach to Central Adrenocortical Insufficiency (CAI) in Thalassemia

The experience of a tertiary unit on the clinical phenotype and management of hypogonadism in female adolescents and young adults with transfusion dependent thalassemia

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

Serum α-klotho levels are not informative for the evaluation of growth hormone secretion in short children

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

Penile length and genital anomalies in Egyptian male newborns: epidemiology and influence of endocrine disruptors

A clinical approach to benign breast lesions in female adolescents

Uterine development in patients with Turner syndrome: Relation to hormone replacement therapy and karyotype

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

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

Pegvisomant-primed growth hormone (GH) stimulation test is useful in identifying true GH deficient children

Pegvisomant-primed growth hormone (GH) stimulation test is useful in identifying true GH deficient children

Effect of GnRH analogue on height potential in patients with severe growth hormone insensitivity syndrome treated with IGF-I

Does Testosterone Replacement Therapy Promote an Augmented Risk of Thrombotic Events in Thalassemia Major Male Patients with Hypogonadism?

Current practice in treating adult female thalassemia major patients with hypogonadism: An International Network of Clinicians for Endocrinopathies in Thalassemia and Adolescence Medicine survey from Italy

Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre

Ovarian reserve and fertility parameters in post-pubertal females with congenital adrenal hyperplasia: a case-control study

THE ICET-A SURVEY ON CURRENT CRITERIA USED BY CLINICIANS FOR THE ASSESSMENT OF CENTRAL ADRENAL INSUFFICIENCY IN THALASSEMIA: ANALYSIS OF RESULTS AND RECOMMENDATIONS

Insulin resistance in obese pre-pubertal children: Relation to body composition

The recommendation of the International Network of Clinicians for Endocrinopathies in Thalassemia and Adolescent Medicine for the assessment of growth hormone secretion in thalassemia

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