Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Nassih, H."'
Autor:
Hammoud, M., Rodrigues, A.M.S., Assiri, I., Sabir, Es, Lafhal, K., Najeh, S., Jakani, M., Imad, N., Bourrahouat, A., Ait Sab, I., Elqadiry, R., Nassih, H., Outzourit, A., Elamiri, M., Maoulainine, F., Slitine Elidrissi, N., Bennaoui, F., Bourous, M., Mrhar, S., Essaadouni, L., Stien, D., Rada, N., Bouskraoui, M., Houël, E., Fdil, N.
Publikováno v:
In Prostaglandins and Other Lipid Mediators October 2023 168
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 14 (2021)
Context: Intussusception is the most common cause of small bowel obstruction in children under 4 years of age. Intussusception is not a widely recognized complication of celiac disease. Case Report: We present a clinical case of a 23-month-old boy wi
Externí odkaz:
https://doaj.org/article/5cbf7d2c9144477ca87b873c9837473a
Publikováno v:
Case Reports in Endocrinology.
Turner’s syndrome (TS) is a sex chromosome disorder due to loss of either all or part of the X chromosome, in some or all the cells of the body. Neurofibromatosis type 1 (NF-1) is a multisystemic genetic disorder that is only rarely observed in ass
Publikováno v:
International Journal of Rare Diseases & Disorders. 4
Publikováno v:
Case Reports in Pediatrics. 12/16/2020, p1-3. 3p.
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 14 (2021)
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights. Case Reports
Context: Intussusception is the most common cause of small bowel obstruction in children under 4 years of age. Intussusception is not a widely recognized complication of celiac disease. Case Report: We present a clinical case of a 23-month-old boy wi
Publikováno v:
Case Reports in Endocrinology.
Pituitary stalk interruption syndrome (PSIS) is a very rare entity, and the clinical manifestations are nonspecific. Neonatal cholestasis due to endocrine disorders is rare and poorly recognized. Our case report describes a case of PSIS in a Moroccan
A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
Publikováno v:
Case Reports in Pediatrics.
Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastr
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