Zobrazeno 1 - 10
of 179
pro vyhledávání: '"H Hurvitz"'
Publikováno v:
Gastroenterology Research and Practice, Vol 2009 (2009)
Objective. Atrial Natriuretic Peptide (ANP) has natriuretic and diuretic effects, synthesized and stored in the atrial cells, released in response to stretch of the atrial muscle during increase venous return. Acute gastroenteritis (AGE) causes dehyd
Externí odkaz:
https://doaj.org/article/6e1c22f0315a49c2a5ef325bedd0c121
Publikováno v:
Emerging Infectious Diseases, Vol 5, Iss 5, Pp 723-724 (1999)
Externí odkaz:
https://doaj.org/article/3079f2e30b544c0481c51a159c541883
Publikováno v:
Journal of Neurosurgery: Pediatrics. 2:339-345
Central nervous system medulloepitheliomas are extremely rare and malignant (World Health Organization Grade IV) primitive neuroectodermal tumors (PNETs) that arise in childhood. Unlike other PNETs, medulloepitheliomas have a dismal prognosis, with o
Publikováno v:
Archives of Disease in Childhood. 93:690-694
Objective: To assess the clinical and laboratory features of acute otitis media (AOM) in infants younger than 2 months, to look for factors predicting bacterial otitis, and to evaluate the accuracy of AOM diagnosis among paediatricians. Methods: The
Autor:
A. Halamish, Aharon Klar, Y Berkun, G. Blinder, M. Nadjari, D. Branski, H. Hurvitz, Gila Shazberg, Talia Israeli, Avi Katz
Publikováno v:
The Journal of Pediatrics. 128:850-853
We report 13 patients with 16 episodes of acute lobar nephronia diagnosed in a prospective study that was conducted among 210 hospitalized children with urinary tract infection. In 30 episodes of urinary tract infection, a hypoechogenic or hyperechog
Publikováno v:
Neuropediatrics. 24:103-106
We report a 7-month-old female baby with recent onset of neurological manifestations and mucocutaneous candidiasis. Immunological findings were compatible with severe combined immune deficiency (SCID). Infectious etiology of the central nervous syste
Publikováno v:
Journal of neurosurgery. Pediatrics. 2(5)
Central nervous system medulloepitheliomas are extremely rare and malignant (World Health Organization Grade IV) primitive neuroectodermal tumors (PNETs) that arise in childhood. Unlike other PNETs, medulloepitheliomas have a dismal prognosis, with o
Publikováno v:
European Journal of Pediatrics. 149:709-712
Five of 13 siblings from a Jewish-Ashkenazi family suffered from recurrent Reye-like episodes. During attacks, these patients excreted alpha-keto-adipic, alpha-hydroxy-adipic, and alpha-aminoadipic acids, branched-chain keto acids and saccharopine in
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 18(4)
Background POU1F1, a pituitary-specific transcription factor of the class 1 POU family, is crucial for the development and differentiation of the anterior pituitary gland. Mutations in the POU1F1 gene have been shown to be responsible for a syndrome