Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Amin J. Barakat"'
Publikováno v:
International Journal of Pediatrics, Vol 2012 (2012)
Externí odkaz:
https://doaj.org/article/a6d0699acfda415b919923392dc45fdc
Autor:
Amin J. Barakat
Publikováno v:
International Journal of Pediatrics, Vol 2012 (2012)
Renal disease is a major cause of morbidity and mortality. Pediatric patients with renal disease, especially younger ones may present with nonspecific signs and symptoms unrelated to the urinary tract. Pediatricians, therefore, should be familiar wit
Externí odkaz:
https://doaj.org/article/89884fe2b48243988da5e298b7558380
Publikováno v:
Pediatric Investigation
Importance: The use of the rapid antigen-detection test (RADT) has become the standard of care in the early diagnosis of group A beta-hemolytic Streptococcus (GAS) pharyngitis. Concern has been expressed over increased false positives when the child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf6dde4cb93033eafff685b5a80af9b
https://doi.org/10.1002/ped4.12109
https://doi.org/10.1002/ped4.12109
Autor:
Amin J Barakat
Publikováno v:
Nephrology and Renal Diseases. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0efd7577d4b81295b1dd3655bc069c33
https://doi.org/10.15761/nrd.1000167
https://doi.org/10.15761/nrd.1000167
Publikováno v:
American Journal of Medical Genetics Part A. 176:1341-1348
Barakat syndrome also known as HDR syndrome (Online Mendelian Inheritance in Man [OMIM] 146255), was first described by Barakat et al. in . It is a rare genetic disorder characterized by the triad of hypoparathyroidism "H," sensorineural deafness "D,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::509073b34f7f9ef2f4b09730da2b5fe0
https://doi.org/10.1002/ajmg.a.38693
https://doi.org/10.1002/ajmg.a.38693
Autor:
Amin J. Barakat, H. Gil Rushton
This comprehensive, easy to read reference addresses the clinical implications of congenital anomalies of the kidney and urinary tract (CAKUT) in children. Authored by a panel of internationally recognized pediatric nephrologists and urologists, chap
Autor:
Amin J. Barakat
Publikováno v:
Congenital Anomalies of the Kidney and Urinary Tract ISBN: 9783319292175
About one-third to half of patients with congenital anomalies of the kidney and urinary tract (CAKUT) have one or more associated anomalies of other organ systems including cardiovascular, gastrointestinal, central nervous, skeletal, and genito-repro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::577428c9f88dc19fc47d8f3a5b5c9436
https://doi.org/10.1007/978-3-319-29219-9_16
https://doi.org/10.1007/978-3-319-29219-9_16
Autor:
Amin J. Barakat, H. Gil Rushton
Publikováno v:
Congenital Anomalies of the Kidney and Urinary Tract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::052dace59a6f9a8c9e83d055de91743b
https://doi.org/10.1007/978-3-319-29219-9
https://doi.org/10.1007/978-3-319-29219-9
Autor:
Amin J. Barakat, Douglas T Johnston, D. Hurewitz, Joshua S. Jacobs, William R. Lumry, Henriette Farkas, Marcus Maurer, Mark Davis-Lorton, Teresa Caballero, Richard G. Gower, Emel Aygören-Pürsün, Paula J. Busse
Publikováno v:
The World Allergy Organization Journal
World Allergy Organization Journal, Vol 4, Iss, Pp S9-S21 (2011)
World Allergy Organization Journal, Vol 4, Iss, Pp S9-S21 (2011)
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant disease resulting from a mutation in the C1-inhibitor gene. HAE is characterized by recurrent attacks of intense, massive, localized subcutaneous edema in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d647fd40a728150d6ba99b031ae8c440
http://europepmc.org/articles/PMC3666183
http://europepmc.org/articles/PMC3666183