T Boudhina
Overview
Explore the profile of T Boudhina including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
21
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Recent Articles
1.
Ben Becher S, Cheour M, Ben Hassine L, Hlioui S, Houas F, Ghram N, et al.
Arch Pediatr
. 1998 Mar;
4(11):1107-10.
PMID: 9488746
Background: Brain cysts caused by Echinococcus granulosus are rare; they occur during childhood in endemic areas. Patients: Six children, aged to 8.5-years old (mean age: 5.5 years) were admitted from...
2.
Ben Becher S, Cheour M, Fredj N, Ben Zahra J, Bellagha I, Chaouachi B, et al.
Arch Pediatr
. 1997 Jun;
4(6):581-2.
PMID: 9239277
No abstract available.
3.
Ben Becher S, Ganouni S, Cheour M, Bouaziz A, Boudhina T
Arch Pediatr
. 1994 Dec;
1(12):1115-7.
PMID: 7849898
Background: The spectrum of CHARGE association includes coloboma, heart disease, choanal atresia, retarded growth and development and/or CNS anomalies, genital anomalies and/or hypogonadism and ear anomalies and/or deafness. Case Report:...
4.
Ben Becher S, Gannouni S, Cheour M, Boudhina T
Arch Pediatr
. 1994 May;
1(5):519-20.
PMID: 7951841
No abstract available.
5.
Ben Becher S, Bouaziz A, Harbi M, Hammou A, Boudhina T
Arch Fr Pediatr
. 1993 Aug;
50(7):599-601.
PMID: 8002726
Background: Proteus syndrome is characterized by a range of various manifestations. The main ones are partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly. Urinary tract abnormalities are exceptional. Case...
6.
Khaldi F, Ben Chehida F, Mrabet S, Ben Becher S, Boudhina T, Bennaceur B
Arch Fr Pediatr
. 1993 Jan;
50(1):55-6.
PMID: 8507142
No abstract available.
7.
Ben Becher S, Boukthir S, Hichri A, Harbi M, Ben Osman A, Boudhina T
Pediatrie
. 1993 Jan;
48(1):51-3.
PMID: 8392692
We report on a case of dermatitis herpetiformis in an eight-year-old boy presenting diarrhoea, short stature and characteristic skin rash. Jejunal biopsy showed a partial villous atrophy. The diagnosis was...
8.
Ben Becher S, el Mabrouk J, Debbiche A, Hammou A, Ghram N, Makni S, et al.
Arch Fr Pediatr
. 1992 Nov;
49(9):799-802.
PMID: 1300968
Background: Schwartz-Jampel syndrome is a rare disorder inherited as an autosomal recessive trait and characterized by growth retardation, multiple skeletal abnormalities, myotonia-like muscle disorders and unusual facies. Case Reports: Case...
9.
Ben Becher S, Boukthir S, Ben Chehida F, Bardi I, Kallel J, Ben Ghachem M, et al.
Ann Pediatr (Paris)
. 1992 May;
39(5):309-12.
PMID: 1616249
Tumor-like calcinosis is an infrequent condition whose etiology is poorly understood. Calcifications develop in the subcutaneous tissue neighboring the large joints. All age groups can be affected, although the disease...
10.
Ben Becher S, Zaafouri M, Bardi I, Jaballah N, Besbes M, Kilani T, et al.
Arch Fr Pediatr
. 1992 Feb;
49(2):109-12.
PMID: 1316109
Pneumoblastoma is a rare malignant pulmonary tumor. A new case is reported in a 2 years 5 month-old girl. Because the lack of locoregional extension an isolated surgical excision was...