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1.
[Congenital tyrosinemia: a case report]
A., Hassani; L., Yaacoubi; S., Ettair; T., Meskini; N., Erreimi; N., Mouane; F.B., Bennis.
Revue Marocaine des Maladies de l'Enfant. 2005; (5): 76-77
in French | IMEMR | ID: emr-74522

Subject(s)
Humans , Male , Prenatal Diagnosis , Tyrosinemias/etiology , Congenital Abnormalities
2.
Benign hypertrophic gastritis in child
L., El Yaakoubi; A., Hassani; S., Ettair; N., Erreimi; N., Mouane; F., Bennis.
Revue Marocaine des Maladies de l'Enfant. 2005; (6): 68-69
in French | IMEMR | ID: emr-74539

Subject(s)
Humans , Male , Gastritis, Hypertrophic/therapy , Child
3.
Menkes disease: About one case
N., El Hajoui; S., Ettair; N., Mouane; T., Meskini; N., Erraimi; F., Bouchta.
Revue Marocaine des Maladies de l'Enfant. 2005; (6): 69-70
in French | IMEMR | ID: emr-74540

Subject(s)
Humans , Male , Ceruloplasmin , Copper , Menkes Kinky Hair Syndrome/therapy , Infant
4.
Apert syndrome: a 3 cases report
L., El Mansouri; M., Kabiri; N., Erreimi; T., Meskini; S., Ettair; N., Mouane; F.B., Bennis.
Revue Marocaine des Maladies de L'Enfant. 2005; (7): 49-50
in French | IMEMR | ID: emr-74557

Subject(s)
Humans , Infant , Review
5.
Maladie coeliaque et mineralisation osseuse chez l'enfant
S., Ettair; M., Hida; N., Mouane; F., Bouchta.
Maghreb Medical. 2003; 23 (365): 42-4
in French | IMEMR | ID: emr-63350

Subject(s)
Humans , Calcification, Physiologic , Child , Glutens , Diet , Absorptiometry, Photon
6.
colites inflammatoires chez l'enfant: a propos de 14 cas
M., Hida; N., Mouane; A., Barkat; S., Ettair; N., Erreimi; S., Hajarabi; M., Barahioui; Bouchta, Bennis.
Revue Maghrebine de Pediatrie [La]. 2000; 10 (5): 249-53
in French | IMEMR | ID: emr-55171

Subject(s)
Humans , Male , Female , Inflammatory Bowel Diseases/therapy , Crohn Disease , Colitis, Ulcerative , Colitis , Child
7.
hyperoxalurie hereditaire [oxalose] [a propos d'un cas]
N., Erreimi; N., Mouane; F., Bouchta.
Maroc Medical. 1997; 19 (2): 21-26
in French | IMEMR | ID: emr-45500

ABSTRACT

We report one case primary hyperoxaluria in a fourteen year old child. The diagnosis was possible after the discovery of oxalate of Ca crystals in kidneys and marrow. Our case illustrates some of the clinical and paraclinical characteristics of oxalosis. It also proves how severe the kidney failure could be in this disease. The diagnosis criteria and the therapeutic possibilities that lead to improve this diseasee are also discussed here


Subject(s)
Humans , Genetic Diseases, Inborn/diagnosis , Oxalates
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