Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Mordechai Aladjem"'
Autor:
Gideon Koren, Zehava Chen-Levi, Pascale Burtin, Mordechai Aladjem, Tamir Dagan, Matitiahu Berkovitch, Robert M. Freedom, Tzvy Bistritzer
Publikováno v:
Therapeutic Drug Monitoring. 20:253-256
Digoxin and gentamicin are widely used in pediatric medicine, and therapeutic monitoring is mandatory because of their narrow margin of safety and wide interpatient and intrapatient pharmacokinetic variabilities. Saliva sampling may be of potential i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2df3c07212f0cd5643be28aec475934
https://doi.org/10.1097/00007691-199806000-00003
https://doi.org/10.1097/00007691-199806000-00003
Autor:
Mordechai Aladjem, Sung Han Kim, Wolfram Henn, Cigdem Altay, Terence P. Speed, Steven M. Haffner, John Blangero, Eve L. Bingham, Chi-Bew Chart, Jerry Pelletier, Katarzyna Dziechciowska, Sung Soo Hong, Paul A. Sieving, Kelaginamane Hiriyanna, Jean W. MacCluer, A. Gürgey, D. Castro de Guerra, Majid Ghahremani, Meridee Segal, Cashell E. Jaquish, Julia E. Richards, Chung Choo Lee, H. Arvelo, Young Bae Park, Francisco M. Salzano, Hemant Pawar, A. Rodríguez Larralde, Jae Jin Chae, Tzvy Bistritzer, Shili Lin, Yong Namkoong, Martin Tieder, André Reis, Michał Witt, Wojciech Cichy, M. P. Stern
Publikováno v:
Human Heredity. 46:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b8d685faca2d4e391dd5705a67f5790
https://doi.org/10.1159/000154367
https://doi.org/10.1159/000154367
Publikováno v:
Pediatric Research. 35:372-375
Pseudohypoaldosteronism is a hereditary salt-wasting syndrome usually seen in infancy with weight loss, dehydration, and failure to thrive. The patho-physiologic origin of Pseudohypoaldosteronism is unknown. The defect could be related to the unrespo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cb2ea838091332f9c654ef71399fdc5
https://doi.org/10.1203/00006450-199403000-00021
https://doi.org/10.1203/00006450-199403000-00021
Autor:
Mordechai Aladjem, Tzvy Bistritzer, Menachem Neuman, Moshe Livne, Michael R. Goldberg, Efrat Broide
Publikováno v:
jpme. 20:289-295
The influence of maternal dexamethasone and ritodrine administration during pregnancy on cord blood cortisol and capillary serum glucose concentrations and on the incidence of respiratory distress syndrome (RDS) was studied in 30 premature infants (g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e9331e0986ffd1863c7a554e1878bc2
https://doi.org/10.1515/jpme.1992.20.4.289
https://doi.org/10.1515/jpme.1992.20.4.289
Publikováno v:
Renal failure. 30(1)
A five-year-old boy was evaluated for fever, abdominal pain, vomiting, and diarrhea lasting two days. Chest radiograph revealed a left bronchopneumonia. Metabolic work-up demonstrated phosphaturia, glucosuria, calciuria, proteinuria, profound hypopho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5768c0e6f5f92bc66cb6b0acf2fb5d14
https://pubmed.ncbi.nlm.nih.gov/18197553
https://pubmed.ncbi.nlm.nih.gov/18197553
Autor:
Jeffrey P. Gardner, Mordechai Aladjem, Edward Cragoe, Abraham Aviv, Haruo Tomonari, Goro Tokudome
Publikováno v:
Experimental Biology and Medicine. 194:165-171
A technique is presented to estimate the initial rates of Na(+)-dependent alkalinization of acidified human fibroblasts and platelets and assess the kinetics of the Na+/H+ antiport in these cells. Cytosolic pH (pHi) exhibits an exponential recovery f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14427df41cb7f43bbc33f161b879f975
https://doi.org/10.3181/00379727-194-43073
https://doi.org/10.3181/00379727-194-43073
Autor:
Mordechai Aladjem, Abraham Aviv
Publikováno v:
Cardiovascular Drugs and Therapy. 4:335-342
Racial differences in the regulation of Na+, K+, and Ca2+ have been shown both at the systemic and cellular levels. These include a higher incidence of "salt sensitivity," lower urinary K+ excretion, lower plasma renin activity, and higher circulatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bf467199c7b3f820a98ac4b0ad07f0b
https://doi.org/10.1007/bf02603173
https://doi.org/10.1007/bf02603173
Publikováno v:
Developmental Medicine & Child Neurology. 39:85-87
Visual evoked potentials (VEPs) were performed in a blind fashion in 114 children aged 3 to 17 years with different types of headaches, in order to investigate whether this could be helpful in the diagnosis of migraine versus other types of headaches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad0826928e600213c9b555d60dd55168
https://doi.org/10.1111/j.1469-8749.1997.tb07389.x
https://doi.org/10.1111/j.1469-8749.1997.tb07389.x
Autor:
Joshua Weissgarten, Shai Efrati, Mordechai Aladjem, Victor Dishy, Michael Averbukh, Sylvia Berman, Leonid Feldman, Zhan Averbukh, Leonid Katchko
Publikováno v:
Nephron. Physiology. 99(1)
Background: Amphotericin B may cause acute reduction in renal function. N-acetylcysteine (NAC) has a renoprotective activity in several nephrotoxic renal insults, but its effect on amphotericin-induced renal failure has not been investigated yet. Met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0813ce54b5991951833327d3a2e90bf3
https://pubmed.ncbi.nlm.nih.gov/15637469
https://pubmed.ncbi.nlm.nih.gov/15637469
Autor:
Tzvy, Bistritzer, Eitan, Kerem, Matitiahu, Berkovitch, Micha J, Rapoport, Sandra, Evans, Mordechai, Aladjem
Publikováno v:
Clinical endocrinology. 56(5)
Pseudohypoaldosteronism type 1 (PHA1) is a rare inherited disorder characterized by salt-wasting due to target organ unresponsiveness to mineralocorticoids. PHA1 comprises two clinically and genetically distinct entities; isolated renal and systemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8fd7397eb1fb81ba122a0ccf3d17402
https://pubmed.ncbi.nlm.nih.gov/12030904
https://pubmed.ncbi.nlm.nih.gov/12030904