Home › Researcher directory › Nozha Kallel
Nozha Kallel
Affiliation : Hopital Universitaire Habib Bourguiba
- 10Publications (affiliation in Tunisia)
- 12Total publications
- 254Citations
- 9h-index
Research profile
Nozha Kallel has 10 indexed publications (2010–2022). Their work appears mainly in “Biochemical and Biophysical Research Communications”, “Indian Journal of Endocrinology and Metabolism” and “The Egyptian Journal of Neurology Psychiatry and Neurosurgery”. Their most cited article, “Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency” (2012), has been cited 49 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Metabolism and Genetic Disorders
- Sexual Differentiation and Disorders
- Mitochondrial Function and Pathology
- Adrenal and Paraganglionic Tumors
- Genomics and Rare Diseases
Publications (10)
- Thymic plasmacytoma presenting as polyneuropathy and revealing multiple myeloma: a case report
- Clinical characteristics and outcomes of critically ill COVID-19 patients in Sfax, Tunisia
- Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis
- 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
- Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency
- Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11 β -Hydroxylase Deficiency
- Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy
- A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNAVal mutation
- Adrenocortical Secreting Mass in a Patient with Gardner's Syndrome: A Case Report
Publication venues
- 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
Publications per year
- 20221
- 20211
- 20132
- 20123
- 20112
- 20101
Collaborations
Partner institutions : Hopital Universitaire Hedi Chaker · University of Sfax · Faculty of Medicine of Sfax · Centre of Biotechnology of Sfax · Hospital Fatuma Bourguiba Monastir
Co-authors
- 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
Bibliographic data from OpenAlex (open database).
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