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Kamel Monastiri
Observed names:
K Monastiri,
K. Monastiri,
Monastiri K,
Monastiri, K.,
Monastiri, Kamel
Institutions:
University of Monastir,
Hospital Fatuma Bourguiba Monastir
Observed institutions:
Hôpital Necker-Enfants Malades,
Centre National de la Recherche Scientifique,
University of Monastir,
Hôpital Farhat Hached,
Hopital Universitaire Hedi Chaker,
Laboratoire de Biochimie,
Hôpital Debrousse,
Hospital Fatuma Bourguiba Monastir,
University of Sousse
show all 9
OpenAlex ID:
A5054269710
Interplay of socio-economic factors, consanguinity, fertility, and offspring mortality in Monastir, Tunisia.
2007
·
Emna Kerkeni
, Kamel Monastiri
, et al.
·
PubMed Central
·
55
Primary antiphospholipid syndrome presenting as complicated Henoch-Schonlein purpura
2002
·
K Monastiri
·
Archives of Disease in Childhood
·
48
PDF
Segmental dilatation of the intestine
2006
·
Mohamed Ben Brahim
, Mohsen Belghith
, et al.
·
Journal of Pediatric Surgery
·
47
Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency
2011
·
Toshiyuki Fukao
, Jörn Oliver Sass
, et al.
·
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
·
45
PDF
Influence of Combined CYP3A4 and CYP3A5 Single-Nucleotide Polymorphisms on Tacrolimus Exposure in Kidney Transplant Recipients: A Study According to the Post-Transplant Phase
2015
·
Karim Aouam
, Abdessalem Kolsi
, et al.
·
Pharmacogenomics
·
41
Incidence of mucopolysaccharidoses in Tunisia.
2009
·
Hadhami Ben Turkia
, Néji Tebib
, et al.
·
PubMed
·
41
Association among education level, occupation status, and consanguinity in Tunisia and Croatia.
2006
·
Emna Kerkeni
, Kamel Monastiri
, et al.
·
PubMed Central
·
36
Nosocomial Neonatal Meningitis by Alcaligenes Xylosoxidans Transmitted by Aqueous Eosin
1993
·
Jalel Boukadida
, Kamel Monastiri
, et al.
·
The Pediatric Infectious Disease Journal
·
29
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: Identification and structural characterization of two novel TAT mutations
2006
·
C. Charfeddine
, K. Monastiri
, et al.
·
Molecular Genetics and Metabolism
·
25
Large duplication 4q25–q34 with mild clinical effect
2004
·
Hatem Elghezal
, Halima Sennana Sendi
, et al.
·
Annales de Génétique
·
23
Septicémie à Saccharomyces cerevisiae chez un prématuré traité par Ultra-Levure®
2013
·
F.Z. Chioukh
, H. Ben Hmida
, et al.
·
Médecine et Maladies Infectieuses
·
19
Comorbidity in the Tunisian population
2015
·
L. Romdhane
, O. Messaoud
, et al.
·
Clinical Genetics
·
18
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
2022
·
Elisa Calì
, Sheng-Jia Lin
, et al.
·
Genetics in Medicine
·
17
PDF
La maladie de Gaucher en Tunisie (étude multicentrique)
2003
·
M Chaabouni
, H Aoulou
, et al.
·
La Revue de Médecine Interne
·
17
Sanjad-Sakati syndrome in a Tunisian child
2015
·
E. Kerkeni
, R. Sakka
, et al.
·
Archives de Pédiatrie
·
15
Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis
2007
·
E. Barkaoui
, W. Cherif
, et al.
·
Journal of Inherited Metabolic Disease
·
15
Les fièvres prolongées de l’enfant. Étude rétrospective de 67 cas
2004
·
S. Chouchane
, C.H. Chouchane
, et al.
·
Archives de Pédiatrie
·
15
Pericardial effusion with cardiac tamponade caused by a central venous catheter in a very low birth weight infant
2016
·
Fatma-Zohra Chioukh
, Karim Ben Ameur
, et al.
·
Pan African Medical Journal
·
14
Molecular characterization of maple syrup urine disease patients from Tunisia
2013
·
N. Jaafar
, A. Moleirinho
, et al.
·
Gene
·
14
La déshydratation hypernatrémique chez l'enfant : étude rétrospective de 105 cas
2005
·
S. Chouchane
, H. Fehri
, et al.
·
Archives de Pédiatrie
·
14
Clonality of clinical methicillin-resistant Staphylococcus epidermidis isolates in a neonatal intensive care unit
2006
·
N. Ben Saida
, A. Ferjéni
, et al.
·
Pathologie Biologie
·
13
Fenugreek odour in maple syrup urine disease
1997
·
K. Monastiri
, K. Limame
, et al.
·
Journal of Inherited Metabolic Disease
·
13
Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome
2017
·
Nehla Ghedira
, Lilia Kraoua
, et al.
·
Biology and Medicine
·
12
PDF
Exploration génotypique d’une bouffée épidémique nosocomiale néonatale à Klebsiella pneumoniae productrice de bêtalactamase à spectre étendu
2002
·
J Boukadida
, N Salem
, et al.
·
Archives de Pédiatrie
·
12
[Clinico-biologic and molecular study of mucopolysaccharidosis in central and southern Tunisia].
2001
·
S Laradi
, K Monastiri
, et al.
·
PubMed
·
11
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Works count:
108
Citation count:
800
H-index:
15
I10-index:
27
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