الرئيسية › دليل الباحثين › Saoussen Abroug
Saoussen Abroug
الانتماء : Hôpital Sahloul
- 58منشورات (انتماء تونسي)
- 78مجموع المنشورات
- 420الاستشهادات
- 12مؤشر h
الملف البحثي
لدى Saoussen Abroug 58 منشور(ات) مفهرسة (1989–2026). تُنشر أعماله أساسًا في «Archives de Pédiatrie»، «Médecine et Maladies Infectieuses» و«Journal of Medical Microbiology». أكثر مقالاته استشهادًا هو «Carriage of multidrug-resistant bacteria among pediatric patients before and during their hospitalization in a tertiary pediatric unit in Tu» (2017)، وقد استُشهد به 31 مرة. 2 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Metabolism and Genetic Disorders
- Kidney Stones and Urolithiasis Treatments
- Vasculitis and related conditions
- Renal Diseases and Glomerulopathies
- Dialysis and Renal Disease Management
المنشورات (58)
- Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
- Prevalence of uremic neuropathy and the effect of dialysis in children with end-stage renal disease: A cohort study
- Idiopathic pulmonary hemosiderosis and stroke secondary to protein C deficiency in a child with Down syndrome: a case report
- Pulmonary mucoepidermoid carcinoma in children: a rare diagnosis not to be overlooked – case report
- Turner Syndrome: results of the first Tunisian study group on Turner Syndrome (TuSGOT)
- ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
- Les complications coronaires de la maladie de Kawasaki et ses facteurs de risque : à propos de 65 cas d'enfants tunisien
- Correlation between Children Respiratory Virus Infections and Climate Factors
- Hépatite A en milieu pédiatrique : expérience d’un service d’urgences pédiatriques durant la période de poussée épidémique entre 2017–2018
- Preliminary national report on cystic fibrosis epidemiology in Tunisia: the actual state of affairs
- Unexpected predominance of rotavirus G9P[8] strain in Tunisian adult diarrheal patients
- Molecular characterization of respiratory syncytial virus circulating in Tunisia between 2015 and 2018
- Evaluation of antibody persistence after a four-dose primary hepatitis B vaccination and anamnestic immune response in children under 6 years
- Molecular characterization of group A rotavirus among children aged under 5 years in Tunisia, 2015–2017
- Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease
- Life-threatening subglottic hemangioma in an infant successfully treated with propranolol
- Pyogenic Brain Abscess in Children: A Tunisian Multi-Centric Experience
- Carriage of multidrug-resistant bacteria among pediatric patients before and during their hospitalization in a tertiary pediatric unit in Tunisia
- Unusual clinical outcome of primary Hyperoxaluria type 1 in Tunisian patients carrying 33_34InsC mutation
- Atlanto-axial langerhans cell histiocytosis in a child presented as torticollis
- Clinical and imaging features of malignant infantile osteopetrosis
- Pseudotumoral acute cerebellitis associated with mumps infection in a child
- Intérêt des analogues d’insuline sur l’équilibre du diabète insulinodépendant chez l’enfant
- HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients
- Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1
- Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure
- A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype–phenotype correlation
- Multiplex Minisequencing of theHBBGene: A Rapid Strategy to Confirm the Most Frequentβ-Thalassemia Mutations in the Tunisian Population
- Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
- Aspects radio-cliniques de l’encéphalopathie postérieure réversible chez l’enfant
- PO-0090 Different Aspect Of Precocious Puberty: Clinical Experience And Outcome (8 Cases)
- PO-0059 Central Diabetes Insipidus In Children: Clinical Profile And Etiologies Monocentric Experience (about 10 Cases)
- Une cause rare de méningite récurrente chez l’enfant : la dysplasie cochléovestibulaire
- Kawasaki disease, Mycoplasma pneumoniae infection and anaplastic large cell lymphoma: An uncommon association
- 1503 Acute Disseminated Encephalomyelitis in Children (Eight Cases Reports)
- 353 Is BNP level still correlated to echocardiographic indices in End-stage renal disease children on maintenance hemodialysis?
- Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria
- Relationship of Brain Natriuretic Peptide Concentrations to Left Ventricular Function and Adverse Outcomes in Children With End-Stage Renal Disease Undergoing Hemodialysis
- Novel mutations in steroid-resistant nephrotic syndrome diagnosed in Tunisian children
- Maladie de Kawasaki et infection à Mycoplasma pneumoniae
- Effets de la réduction de la précharge sur les paramètres échographiques de la fonction systolique et diastolique du ventricule gauche de l’enfant en insuffisance rénale terminale : étude comparative avant et après hémodialyse
- Localisation digestive exceptionnelle des dépôts cristallins dans l’hyperoxalurie primitive
- Dépendance de la réponse à la supplémentation vitaminique B du génotype C 677T MTHFR chez les enfants hémodialysés
- Une cause rare de stridor néonatal : la sténose trachéale congénitale
- SFP-P105 – Pédiatrie générale et sociale – L’actinomycose : une cause rare de masses abdominales chez l’enfant
- Manifestations cutanées de l’hyperoxalurie primitive
- SFP-P104 – Pédiatrie générale et sociale – Maladie de Kawasaki et infection Mycoplasma pneumoniae à propos de trois cas
- Hydatidose cérébrale
- A prospective study of the prevalence of heparin‐induced antibodies and other associated thromboembolic risk factors in pediatric patients undergoing hemodialysis
- Apport de la leucoconcentration dans le diagnostic du Kala-azar en Tunisie
- Hépatite A et purpura rhumatoïde : une association rare
- Mastocytose systémique du nourrisson : à propos d’un cas avec atteinte respiratoire et digestive
- Homocystéine et statut antioxydant en hémodialyse pédiatrique
- Les malformations artérioveineuses médullaires chez l’enfant
- Paramètres biochimiques chez les β-thalassémiques
- Entérite à Campylobacter dans le centre tunisien : étude épidémiologique, clinique et bactériologique de quarante cas
- Profil bacteriologique des infections materno-foetales en Tunisie
- Infection hospitaliere a Salmonelles dans un service de Pediatrie generale
مجلات النشر
- Archives de Pédiatrie × 8
- Médecine et Maladies Infectieuses × 5
- Journal of Medical Microbiology × 4
- Immuno-analyse & Biologie Spécialisée × 3
- Pediatric Nephrology × 2
- Annales de Cardiologie et d Angéiologie × 2
المنشورات حسب السنة
- 20261
- 20251
- 20233
- 20221
- 20213
- 20203
- 20193
- 20182
- 20176
- 20164
التعاون العلمي
المؤسسات الشريكة : Hôpital Farhat Hached · University of Sousse · University of Monastir · Hopital Universitaire Hedi Chaker · Hôpital Charles-Nicolle
بلدان المؤلفين المشاركين : فرنسا
المؤلفون المشاركون
- Jalel Chemli
- Saida Hassayoun
- Azza Harbi
- Houda Ajmi
- Noura Zouari
- Miniar Tfifha
- Asma Omezzine
- Sameh Mabrouk
- Ali Bouslama
- Ibtihel Benhaj Mbarek
- Nouri Zouari
- Noureddine Boujâafar
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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