الرئيسية › دليل الباحثين › Kamel Monastiri
Kamel Monastiri
الانتماء : University of Monastir · Hospital Fatuma Bourguiba Monastir
- 69منشورات (انتماء تونسي)
- 108مجموع المنشورات
- 800الاستشهادات
- 15مؤشر h
الملف البحثي
لدى Kamel Monastiri 69 منشور(ات) مفهرسة (1993–2026). تُنشر أعماله أساسًا في «Archives de Pédiatrie»، «Pathologie Biologie» و«Médecine et Maladies Infectieuses». أكثر مقالاته استشهادًا هو «Primary antiphospholipid syndrome presenting as complicated Henoch-Schonlein purpura» (2002)، وقد استُشهد به 48 مرة. 7 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا، البرتغال.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Metabolism and Genetic Disorders
- Genomics and Rare Diseases
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Neonatal and Maternal Infections
المنشورات (69)
- Using Exome Sequencing to Identify the Causes of Neurodevelopmental Disorders: Experience of a North African Genetic Center
- Risk factors, outcomes, and predictors of therapeutic response in preterm infants with patent ductus arteriosus: A retrospective cohort study
- Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
- Short-term outcomes and predictive factors of mortality among Very Low Birth Weight newborns (< 1500g): cross-sectional study in the Neonatal Intensive Care Unit of Monastir, Tunisia.
- Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy: QARS1 new variants associated with a severe phenotype in a patient
- Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007–2021)
- Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy: QARS1 variants associated with a severe phenotype in a patient
- Turner Syndrome: results of the first Tunisian study group on Turner Syndrome (TuSGOT)
- First description of the MEGDEHL syndrome in the Tunisian population via whole‐exome sequencing: Novel nonsense mutation inSERAC1gene
- Mandibuloacral dysplasia type A in five tunisian patients
- Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients
- Primary Pulmonary Hypertension Associated with Asymptomatic Methylmalonic Aciduria in a Child
- Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome
- Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome
- ABCB1 and SLCO1B3 Gene Polymorphisms and Their Impact on Digoxin Pharmacokinetics in Atrial Fibrillation Patients among the Tunisian Population
- Therapeutic drug monitoring of caffeine in preterm infants: Could saliva be an alternative to serum?
- Pericardial effusion with cardiac tamponade caused by a central venous catheter in a very low birth weight infant
- Duodenal Atresia Associated with Apple Peel Atresia and Situs Inversus Abdominus: A Case Report
- Fiabilité de la mesure de la glycémie capillaire par rapport à la glycémie plasmatique chez le nouveau-né
- Spontaneous Intestinal Perforation in a Very Low Birth Weight Infant: Successful Management by Peritoneal Needle Suction
- Détresse respiratoire révélant un corps étranger intra-œsophagien chez un nouveau-né
- Méningite néonatale à méningocoque : à propos d’une observation tunisienne d’évolution fatale
- Une cause inhabituelle de détresse respiratoire chez un nouveau-né
- Réponse à la lettre à l’éditeur du Dr S. Lemoine et al. à propos de la publication « Fiabilité de la mesure de la glycémie capillaire par rapport à la glycémie plasmatique chez le nouveau-né »
- Influence of Combined CYP3A4 and CYP3A5 Single-Nucleotide Polymorphisms on Tacrolimus Exposure in Kidney Transplant Recipients: A Study According to the Post-Transplant Phase
- Comorbidity in the Tunisian population
- Sanjad-Sakati syndrome in a Tunisian child
- Molecular characterization of piebaldism in a Tunisian family
- Hyperthyroïdie néonatale et maladie de Basedow maternelle
- Morbidité respiratoire des prématurés tardifs dans une unité de soins intensifs néonatale
- Diagnostic anténatal des malformations digestives
- PO-0739 An Unusual Case Of Neonatal Respiratory Distress : Case Report
- Diagnostic anténatal des malformations digestives
- Multicentric neonatal myofibromatosis
- Septicémie à Saccharomyces cerevisiae chez un prématuré traité par Ultra-Levure®
- Molecular characterization of maple syrup urine disease patients from Tunisia
- Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency
- A novel CASR mutation in a Tunisian FHH/NSHPT family associated with a mental retardation
- Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
- 461 The First Six Years Experience of Tunisian Congenital Anomalies Registry
- Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
- Analyse moléculaire de la mutation p.Asn 370 Ser dans la maladie de Gaucher
- Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis
- Segmental dilatation of the intestine
- Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: Identification and structural characterization of two novel TAT mutations
- Clonality of clinical methicillin-resistant Staphylococcus epidermidis isolates in a neonatal intensive care unit
- Ecthyma gangréneux : 3 cas
- Are low doses of enoxaparin with aspirin sufficient to guarantee good gestational outcome in women with heterozygote factor V Leiden mutation?
- La déshydratation hypernatrémique chez l'enfant : étude rétrospective de 105 cas
- Infantile abdominal aortic aneurysms: Report of two cases
- Large duplication 4q25–q34 with mild clinical effect
- Les fièvres prolongées de l’enfant. Étude rétrospective de 67 cas
- Prevalence in a Tunisian Arabic population of factor VII DNA variants and relation to factor VII plasma levels
- La maladie de Gaucher en Tunisie (étude multicentrique)
- Primary antiphospholipid syndrome presenting as complicated Henoch-Schonlein purpura
- Exploration génotypique d’une bouffée épidémique nosocomiale néonatale à Klebsiella pneumoniae productrice de bêtalactamase à spectre étendu
- [Rapid detection of BRCA-1 germline mutations by the protein truncation test in Tunisian families].
- Sanfilippo disease type B and neonatal supraventricular tachycardia
- Incidence of mucopolysaccharidoses in central and south Tunisia
- Syndromes hémorragiques du nouveau-né
- Résistance du facteur V à la protéine C activée au cours des avortements à répétition
- β‐Ketothiolase (2‐methylacetoacetyl‐CoA thiolase) deficiency: A frequent disease in Tunisia?
- Alcaligenes xylosoxydans: l'origine de l'infection est le plus souvent une solution d'antiseptique
- Aspects épidémiologiques de la résistance des entérobactéries aux céphalosporines de troisième génération en Tunisie Centrale (étude rétrospective sur 3 ans)
- [Primary antiphospholipid syndrome in obstetrics. Apropos of 4 cases with fetal survival].
- [Mitochondrial myopathies. Diagnostic approaches and genetic counseling].
- La listériose humaine en Tunisie : deux nouveaux cas chez le nouveau-né
- Entérite à Campylobacter dans le centre tunisien : étude épidémiologique, clinique et bactériologique de quarante cas
- NOSOCOMIAL NEONATAL MENINGITIS BY ALCALIGENES XYLOSOXIDANS TRANSMITTED BY AQUEOUS EOSIN
مجلات النشر
- Archives de Pédiatrie × 13
- Pathologie Biologie × 4
- Médecine et Maladies Infectieuses × 4
- PubMed × 3
- Clinical Genetics × 2
- Research Square × 2
المنشورات حسب السنة
- 20263
- 20251
- 20243
- 20231
- 20221
- 20211
- 20201
- 20191
- 20181
- 20173
التعاون العلمي
المؤسسات الشريكة : Hôpital Farhat Hached · Hôpital La Rabta · Tunis El Manar University · Institut Pasteur de Tunis · Faculté de médecine de Tunis
بلدان المؤلفين المشاركين : فرنسا · البرتغال
المؤلفون المشاركون
- Fatma Zohra Chioukh
- Hayet Ben Hamida
- K. Ben Ameur
- Emna Kerkeni
- Jalel Boukadida
- Sonia Abdelhak
- Noureddine Snoussi
- Mohamed Neji Guediche
- Manel Bizid
- Néji Tebib
- Naziha Kaabachi
- Rania Sakka
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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