الرئيسية › دليل الباحثين › Jalel Chemli
Jalel Chemli
الانتماء : Hôpital Sahloul
- 68منشورات (انتماء تونسي)
- 78مجموع المنشورات
- 1241الاستشهادات
- 15مؤشر h
الملف البحثي
لدى Jalel Chemli 68 منشور(ات) مفهرسة (2002–2026). تُنشر أعماله أساسًا في «Archives de Pédiatrie»، «PubMed» و«Journal of Clinical Immunology». أكثر مقالاته استشهادًا هو «X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production» (2006)، وقد استُشهد به 282 مرة. 5 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Immunodeficiency and Autoimmune Disorders
- Metabolism and Genetic Disorders
- Vasculitis and related conditions
- Tuberculosis Research and Epidemiology
- Autoimmune and Inflammatory Disorders Research
المنشورات (68)
- Comparing video-based and four-step simulation training in paediatric basic life support: a pilot randomised controlled study
- Epidemiological, Bacteriological, and Evolutive Features of Children Hospitalized for Infective Endocarditis in a Tertiary Tunisian Pediatric Department
- PP203 Topic: AS19–Other: Ethics/Endocrine/Metabolism/Burns/Genetics/Rheumatology/Other: EPIDEMIOLOGICAL, CLINICAL, AND SHORT-TERM OUTCOME STUDY OF SEVERE BURNS IN CHILDREN: A REPORT ON 152 CASES
- PP310 Topic: AS06–Extracorporeal Organ Support: ECMO/Ventricular Assist Devices (Temporary & Durable)/MARS/Total Plasma Exchange/Plasmapheresis/Other: ASSESSMENT OF CENTRAL VENOUS CATHETER UTILIZATION AND COMPLICATION IN A TUNISIAN TERTIARY PEDIATRIC INTENSIVE CARE UNIT
- PP311 Topic: AS06–Extracorporeal Organ Support: ECMO/Ventricular Assist Devices (Temporary & Durable)/MARS/Total Plasma Exchange/Plasmapheresis/Other: THERAPEUTIC PLASMA EXCHANGE IN PEDIATRIC INTENSIVE CARE UNIT: A TUNISIAN SINGLE-CENTER EXPERIENCE
- Idiopathic pulmonary hemosiderosis and stroke secondary to protein C deficiency in a child with Down syndrome: a case report
- Clinical and radiological findings of posterior reversible encephalopathy syndrome in children: About 16 children hospitalized in the pediatric department of a Tunisian tertiary care hospital
- Les complications coronaires de la maladie de Kawasaki et ses facteurs de risque : à propos de 65 cas d'enfants tunisien
- Acute disseminated encephalomyelitis: A retrospective study of 20 children in a pediatrics department in Tunisia
- Hépatite A en milieu pédiatrique : expérience d’un service d’urgences pédiatriques durant la période de poussée épidémique entre 2017–2018
- Vein of Galen Aneurysmal Malformation revealed by a severe heart failure and pulmonary hypertension in an infant
- Success of anti-CD20 monoclonal antibody treatment for severe autoimmune hemolytic anemia caused by warm-reactive immunoglobulin A, immunoglobulin G, and immunoglobulin M autoantibodies in a child: a case report
- 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
- Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
- X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
- A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients
- Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1
- Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)
- Acute myocarditis associated with parvovirus B19 infection in a child
- Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
- PO-0251 Tuberculosis In Children: A Study Of 32 Cases
- PO-0081 Pituitary Stalk Interruption Syndrome: Clinical, Radiologic And Therapeutic Particularity
- PO-0059 Central Diabetes Insipidus In Children: Clinical Profile And Etiologies Monocentric Experience (about 10 Cases)
- PO-0379 Different Aspect Of Childhood Langherhans Cell Histiocytosis : Experience From A Single Centre
- Une cause rare de méningite récurrente chez l’enfant : la dysplasie cochléovestibulaire
- Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients
- Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa
- A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients
- Diagnostic moléculaire de la maladie de Gaucher en Tunisie
- Kawasaki disease, Mycoplasma pneumoniae infection and anaplastic large cell lymphoma: An uncommon association
- 1503 Acute Disseminated Encephalomyelitis in Children (Eight Cases Reports)
- Maladie de Kawasaki et infection à Mycoplasma pneumoniae
- Gaucher disease in Tunisia: High frequency of the most common mutations
- Traitement du syndrome néphrotique idiopathique corticorésistant
- Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
- [Complete primary distal renal tubular acidosis in children: 11 cases].
- SFP-P210 – Néphrologie – Syndrome néphrotique idiopathique corticorésistant de l’enfant : étude de 20 cas
- SFCE-P17 – Hématologie, immunologie – Aspects cliniques et étiologiques des bécégites disséminées en Tunisie
- [Uremic and haemolytic syndrome in children: study of 17 cases].
- 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
- SFP-P104 – Pédiatrie générale et sociale – Maladie de Kawasaki et infection Mycoplasma pneumoniae à propos de trois cas
- SFP-P103 – Néphrologie – Aspects cliniques et évolutifs du syndrome de Bartter dans la région centrale de la Tunisie à propos de neuf cas
- [Pediatric celiac disease in the region of Sousse: epidemiological and evolutive study of 80 cases].
- [Graves's disease in children and adolescent: study of seven cases].
- DISSEMINATED BCG INFECTION IN TUNISIA: CLINICAL AND AETIOLOGICAL FEATURES
- Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis
- Syndrome opsoclonie–myoclonie associé à une infection à Mycoplasma pneumoniae
- [Primary hyperoxaluria in children in central Tunisia].
- [Lupus nephritis in childhood: clinical and evolutive study of 14 cases].
- [Henoch Schonlein purpura in children: clinical and evolutive study of 122 cases].
- X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production
- Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
- Rhombencephalosynapsis diagnosed in childhood: Clinical and MRI findings
- Apport de la leucoconcentration dans le diagnostic du Kala-azar en Tunisie
- Maladie de basedow associée a une maladie cœliaque chez une adolescente trisomique 21
- [Mycobacterial infections in children in Central Tunisia. A study of 31 cases including 7 disseminated BCG-osis].
- Les fièvres prolongées de l'enfant : à propos de 110 cas
- [Clinical features and course of Kawasaki disease in central Tunisia: a study about 14 cases collected over a period of three years (2000-2002)].
- [Indications and outcomes of surgical treatment of gastro-duodenal ulcer in child and adolescent. About 45 cases].
- Hépatite A et purpura rhumatoïde : une association rare
- [Accidental caustic ingestion in Tunisian child. Study of 330 cases].
- Purpura rhumatoïde et tuberculose rénale
- Connectivite mixte révélée par une méningite lymphocytaire chronique chez un nourrisson
- Mastocytose systémique du nourrisson : à propos d’un cas avec atteinte respiratoire et digestive
- Clinical and Genetic Heterogeneity of Inherited Autosomal Recessive Susceptibility to DisseminatedMycobacterium bovisBacille Calmette‐Guérin Infection
مجلات النشر
- Archives de Pédiatrie × 12
- PubMed × 11
- Journal of Clinical Immunology × 4
- Pediatric Critical Care Medicine × 3
- Journal of Medical Case Reports × 2
- European Journal of Paediatric Neurology × 2
المنشورات حسب السنة
- 20261
- 20244
- 20232
- 20213
- 20181
- 20174
- 20164
- 20152
- 20146
- 20133
التعاون العلمي
المؤسسات الشريكة : Institut Pasteur de Tunis · Hôpital La Rabta · Tunis El Manar University · Hôpital Farhat Hached · Faculté de médecine de Tunis
المؤلفون المشاركون
- Houda Ajmi
- Saida Hassayoun
- Saoussen Abroug
- Azza Harbi
- Noura Zouari
- Sameh Mabrouk
- Saoussan Abroug
- Mohamed‐Ridha Barbouche
- Sonia Abdelhak
- Meriem Ben‐Ali
- Miniar Tfifha
- Fadoua Majdoub
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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