الرئيسية › دليل الباحثين › Nozha Kallel

Nozha Kallel

الانتماء : Hopital Universitaire Habib Bourguiba

• 10منشورات (انتماء تونسي)
• 12مجموع المنشورات
• 254الاستشهادات
• 9مؤشر h

OpenAlex

مجالات البحث

• Metabolism and Genetic Disorders
• Sexual Differentiation and Disorders
• Mitochondrial Function and Pathology
• Adrenal and Paraganglionic Tumors
• Genomics and Rare Diseases

المنشورات (10)

• Thymic plasmacytoma presenting as polyneuropathy and revealing multiple myeloma: a case report
  2022 · The Egyptian Journal of Neurology Psychiatry and Neurosurgery
• Clinical characteristics and outcomes of critically ill COVID-19 patients in Sfax, Tunisia
  2021 · Acute and Critical Care · استُشهد به 10 مرة
• Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis
  2013 · Indian Journal of Endocrinology and Metabolism · استُشهد به 24 مرة
• A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions
  2013 · Biochemical and Biophysical Research Communications · استُشهد به 21 مرة
• Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency
  2012 · The American Journal of the Medical Sciences · استُشهد به 49 مرة
• Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11 β -Hydroxylase Deficiency
  2012 · Case Reports in Urology · استُشهد به 19 مرة
• Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  2012 · Indian Journal of Endocrinology and Metabolism · استُشهد به 17 مرة
• The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy
  2011 · Biochemical and Biophysical Research Communications · استُشهد به 26 مرة
• A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNAVal mutation
  2011 · Biochemical and Biophysical Research Communications · استُشهد به 6 مرة
• Adrenocortical Secreting Mass in a Patient with Gardner's Syndrome: A Case Report
  2010 · Case Reports in Medicine · استُشهد به 12 مرة

مجلات النشر

• Biochemical and Biophysical Research Communications × 3
• Indian Journal of Endocrinology and Metabolism × 2
• The Egyptian Journal of Neurology Psychiatry and Neurosurgery × 1
• Acute and Critical Care × 1
• The American Journal of the Medical Sciences × 1
• Case Reports in Urology × 1

المنشورات حسب السنة

• 20221
• 20211
• 20132
• 20123
• 20112
• 20101

التعاون العلمي

المؤسسات الشريكة : Hopital Universitaire Hedi Chaker · University of Sfax · Faculty of Medicine of Sfax · Centre of Biotechnology of Sfax · Hospital Fatuma Bourguiba Monastir

المؤلفون المشاركون

• Nadia Charfi
• Mouna Feki Mnif
• Fatma Mnif
• Zainab Mnif
• Nabila Mejdoub Rekik
• Mahdi Kamoun
• Mohamed Abid
• Faiza Fakhfakh
• Mongia Hachicha
• Emna Mkaouar‐Rebai
• Najla Mezghani
• Emna Daoud

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).