Search Results - "Sfar, M. H"

Arthralgia is the main associated symptom to anxio-depressive disorders during the “Long COVID” among Tunisian patients by Zaouali, F, Chaouch, A, Boubaker, F, Bouchareb, S, Mrabet, H E, A Ben Mabrouk, Touil, I, Boussoffara, L, Knani, J, Boudawara, N, Alaya, W, Sfar, M H

“…IntroductionVarious psychiatric disorders were reported during the long COVID. The most frequently cited by physicians included the insomnia, the…”
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Organic and psychiatric symptoms of “Long COVID” among Tunisian patients: a cross sectional study by Zaouali, F., Chaouch, A., Boubaker, F., Bouchareb, S., Mrabet, H. E., Ben Mabouk, A., Touil, I., Boussofara, L., Knani, J., Boudawara, N., Alaya, W., Sfar, M. H.

“…Introduction Long COVID is a condition characterized by long-term health problems persisting or appearing after the typical recovery period of COVID-19…”
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Risk assessment for foot ulcers among Tunisian subjects with diabetes: a cross sectional outpatient study by Zantour, B, Bouchareb, S, El Ati, Z, Boubaker, F, Alaya, W, Kossomtini, W, Sfar, M. H

“…Abstract Background Diabetic foot is an underestimated and redoubtable diabetes complication. The aims of our study were to assess diabetic foot ulcer risk…”
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Association between depression and insulintherapy by Zaouali, F., El Khemiri, A., Boubaker, F., Arfa, S., Zantour, B., Alaya, W., Sfar, M. H.

“…Introduction Insulin is the basic medical therapy to manage type 1 diabetes and is also a cornerstone of treatment of type 2 diabetes as insulinopenia belongs…”
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Benzylthiouracil-induced antineutrophil cytoplasmic antibody-associated cutaneous vasculitis: a case report and literature review by Chebbi, W, Zantour, B, Alaya, W, Belhadjali, H, Sfar, M H

“…Vasculitis associated to antineutrophil cytoplasmic antibodies is a rare complication of therapy with antithyroid medication. They were mainly reported in…”
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Muscular dystrophy associated with isolated neurosarcoidosis: A case report by Cherif, Y, Younes, S, Kossomtini, W, Alaya, W, Zantour, B, Jerbi, S, Sfar, M.-H

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Tuberous sclerosis and intracranial aneurysms: a rare association by Aissi, M, Younes-Mhenni, S, Jerbi-Ommezzine, S, Boughammoura-Bouatay, A, Frih-Ayed, M, Sfar, M H

“…Tuberous sclerosis is an autosomal dominant inherited phakomatosis. It is associated with a wide variety of central nervous system abnormalities, but…”
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Maladie de Behçet juvénile : à propos de quatre observations by Chebbi, W., Jerbi Omezzine, S., Ammari, W., Mahjoub, B., Sfar, M.H.

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Depression among type 2 diabetic insulin-dependent older adults by Zaouali, F., Lassoued, N., Boubaker, F., Alaya, W., Sfar, M.H.

“…Introduction Although depression is one of the most common diseases among older people, it is still underdiagnosed due to frequent misleading symptoms…”
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Determinants of insulin treatment satisfaction among type 2 diabetic older adults by Zaouali, F., Lassoued, N., Sondess, A., Alaya, W., Sfar, M.H.

“…Introduction Glycemic control for elderly diabetics is a challenge. Treatment satisfaction reflects this control. Objectives To determine the factors…”
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Werner's syndrome and endocrine disorders by Zantour, B, Messaoud, R, Zouali, M, Ladjimi, A, Braham, H, Hamza, H, Zebidi, A, Sfar, M H

“…Werner's syndrome is a rare autosomal recessive disease caused by the mutation of DNA helicase gene (WRN), characterized by the premature onset of multiple…”
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Iron deficiency anemia in people aged 65 years and older: a cohort study of 102 patients by Chebbi, W, Arfa, S, Zantour, B, Sfar, M H

“…Iron deficiency anemia is a common hematological abnormality in the older people. The aim of this study is to determine the clinical and biological…”
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Hashimoto's thyroiditis and severe hypothyroidism, associated with a single hot nodule by Zantour, B, Sfar, M.H, Alaya, W, Chebbi, W, Chatti, K, Jerbi, S

“…Abstract We report the case of a 27 year-old man with symptoms of severe hypothyroidism that have evolved since his adolescence. He was found to have an 11 mm…”
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Familial idiopathic pulmonary fibrosis associated with autoimmune polyendocrinopathy and epidermodysplasia verruciformis by Zantour, B, Knani, J, Boudawara, N, Boussoffara, L, Jerbi, S, Hamza, H, Laarif, M, Mlika, S, Sfar, M H

“…Familial idiopathic pulmonary fibrosis (IPF) is a very rare and progressively fatal disease. Its pathogenesis is not fully understood and involves damage to…”
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Serum copper, zinc and selenium levels in Tunisian patients with Parkinson's disease by Younes-Mhenni, S, Aissi, M, Mokni, N, Boughammoura-Bouatay, A, Chebel, S, Frih-Ayed, M, Kerkeni, A, Bost, M, Chazot, G, Sfar, M T, Sfar, M H

“…Parkinson's disease (PD) is a progressive neurodegenerative disorder. The etiology of this disease is still not fully clear, but free radicals have been…”
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Vascularite cutanée à anticorps anti-cytoplasme des polynucléaires neutrophiles induite par le benzylthio-uracile : à propos d’un cas et revue de la littérature by Chebbi, W., Zantour, B., Alaya, W., Belhadjali, H., Sfar, M.H.

“…Les vascularites à anticorps anti-cytoplasme des polynucléaires neutrophiles constituent une complication rare des antithyroïdiens de synthèse. Elles sont…”
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Thrombopénie ferriprive : un diagnostic différentiel rare du purpura thrombopénique auto-immun by Chebbiz, W., Machraoui, R., Souissi, J., Zantour, B., Kili, R., Harzallah, O., Mahjoub, S., Sfar, M.-H.

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Regression of visual disorders under bromocriptine in patients with prolactin-secreting macroadenoma by Chaieb, L, Chadli-Chaieb, M, Sfar, M H, Ach, K, Zebidi, A, Kacem, M

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Anévrismes intracrâniens et sclérose tubéreuse de Bourneville : une association rare by Aissi, M., Younes-Mhenni, S., Jerbi-Ommezzine, S., Boughammoura-Bouatay, A., Frih-Ayed, M., Sfar, M.H.

“…La sclérose tubéreuse de Bourneville (STB) est une phacomatose se compliquant fréquemment de manifestations neurologiques. Nous rapportons l’observation d’un…”
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Idiopathic intracranial hypertension and factor V Leiden mutation by Younes, S, Aissi, M, Chérif, Y, Daoussi, N, Boughammoura, A, Frih Ayed, M, Sfar, M H, Jerbi, S

“…Activated proteinC resistance is a frequent prothrombotic abnormality. In most cases it is due to factorV Leiden mutation by nucleotide G1691A substitution…”
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