Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Manoochehr Karjoo"'
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 12, Pp 6469-6484 (2017)
Familial Mediterranean fever, an autosomal recessive disorder, is a member of the periodic fever syndromes, and considered to be the most common cause of recurrent febrile episodes in children. It is important to understand the disorder as familial M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::fb644a5c13be98eac09e6a085d1f9e7c
http://ijp.mums.ac.ir/article_9501_c8c72993abe110f66b167adc1cb797e4.pdf
http://ijp.mums.ac.ir/article_9501_c8c72993abe110f66b167adc1cb797e4.pdf
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 10, Pp 5805-5808 (2017)
Elevated enzyme activities in plasma may at times be attributed to the presence of macro-enzymes. The macro-enzymes are often serum enzymes in complex with immunoglobulins, resulting in a greater molecular mass that cannot be filtered by renal glomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::bc604df131895e68b6a33c1976560044
http://ijp.mums.ac.ir/article_9103_42dae51d73b54ac65687fc741da5a03f.pdf
http://ijp.mums.ac.ir/article_9103_42dae51d73b54ac65687fc741da5a03f.pdf
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 10, Pp 5881-5886 (2017)
We are reporting an infant with persistent abnormal liver function, neonatal jaundice, and intermittent hypoglycemia. Evaluation confirmed congenital hypopituitarism, in the absence of congenital anomalies and midline defect. His jaundice and abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::3b03f08185fa5f8149d9d6e5d8681e6a
http://ijp.mums.ac.ir/article_9143_0d54290f59ef4fa37795546eda8b7c2d.pdf
http://ijp.mums.ac.ir/article_9143_0d54290f59ef4fa37795546eda8b7c2d.pdf
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 5, Pp 4849-4853 (2017)
Myasthenia gravis (MG) is an autoimmune disease resulting in destruction of the post-synaptic nicotinic receptors at the neuromuscular junction. Classically, the earliest symptoms of MG are ocular, including ptosis and diplopia. Other less common ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::fede743d4e042facf0e314ced615ebeb
http://ijp.mums.ac.ir/article_8499_42259a14cbd3f45e87438fc3701e8ba8.pdf
http://ijp.mums.ac.ir/article_8499_42259a14cbd3f45e87438fc3701e8ba8.pdf
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 3, Pp 4449-4455 (2017)
The ingestion of foreign bodies is a comprehensive problem affecting the pediatric population, especially under 5 years of age. The ingestion of 2 or more magnets may lead to their attraction over planes of intervening soft tissue with enough force t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::36b4161d25040fa71abceeb989f0b8cb
http://ijp.mums.ac.ir/article_8263_09663fb41b650655fcd352d1a267a558.pdf
http://ijp.mums.ac.ir/article_8263_09663fb41b650655fcd352d1a267a558.pdf
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 1, Pp 4233-4237 (2017)
Familial adenomatous polyposis (FAP) is a hereditary autosomal dominant cancer syndrome, results from germ line mutation or deletion of the Adenomatous Polyposis Coli (APC) gene on chromosome 5q21. Patients with FAP suffer from multiple polyps mainly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::e34ce9e29c342bac259846d4966b8e7c
http://ijp.mums.ac.ir/article_8040_077c79ec66deb11117eb879232afba15.pdf
http://ijp.mums.ac.ir/article_8040_077c79ec66deb11117eb879232afba15.pdf
Publikováno v:
International Journal of Pediatrics, Vol 6, Iss 3, Pp 7271-7273 (2018)
A digital rectal examination is a highly important procedure carried out on infants and children during visits to the gastroenterology clinic, but is often accompanied with physiologic and psychologic trauma in patients, along with being diagnostical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::f4313b209c87e366e5303e8f65796151
http://ijp.mums.ac.ir/article_10320_f14b6c1e74dbc5d96f1ee7390677432a.pdf
http://ijp.mums.ac.ir/article_10320_f14b6c1e74dbc5d96f1ee7390677432a.pdf
Publikováno v:
International Journal of Pediatrics, Vol 4, Iss 9, Pp 3399-3404 (2016)
Crohn’s disease is an inflammatory bowel disease (IBD), characterized by chronic intestinal inflammation that causes the loss of immune tolerance leading to bizarre inflammatory signals and disruption of mucosal barriers. Environmental triggers and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::174f3e95ff2e75c91eb217f0b5a6f673
http://ijp.mums.ac.ir/article_7334_c0c47553429c0959e420da970cf1667c.pdf
http://ijp.mums.ac.ir/article_7334_c0c47553429c0959e420da970cf1667c.pdf
Publikováno v:
International Journal of Pediatrics, Vol 4, Iss 8, Pp 2287-2293 (2016)
Gaucher Disease (GD) is the most common type of Lysosomal Storage Disorder and it is divided into three distinct subtypes. The authors here report four different cases of Gaucher Disease, with varying clinical manifestations, and the diagnosis of eac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::81263afc9f877bab9e2a7d81a24aa621
http://ijp.mums.ac.ir/article_7307_2840eca42262c5930dcf11661a6b00ec.pdf
http://ijp.mums.ac.ir/article_7307_2840eca42262c5930dcf11661a6b00ec.pdf
Publikováno v:
International Journal of Pediatrics, Vol 4, Iss 8, Pp 3293-3298 (2016)
Background To this date, there has been no specific therapy proven to be effective for cyclic vomiting syndrome (CVS) in controlled trials. Multiple regimens have been proposed including: cyproheptadine, propranolol, amitriptyline, and phenobarbital.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::1d42526c9a0949a471d35cd2e94176c8
http://ijp.mums.ac.ir/article_7187_e528a44737c70fb6f2aba475e3c9bc1f.pdf
http://ijp.mums.ac.ir/article_7187_e528a44737c70fb6f2aba475e3c9bc1f.pdf