Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ricardo Guirola"'
Autor:
Shelley Watts, Maranda Diaz, Christa Teller, Tyler Hamby, Ricardo Guirola, Maria Perez, Gretchen Eames, Richard Howrey, Ana Rios, Heidi Trinkman, Anish Ray
Publikováno v:
Journal of Pediatric Hematology/Oncology. 45:e328-e333
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e83695f05067a219d2c7ba0ca07c3a
https://doi.org/10.1097/mph.0000000000002602
https://doi.org/10.1097/mph.0000000000002602
Hemophagocytic lymphohistiocytosis (HLH) is a rare yet potentially fatal systemic disease arising from uncontrolled activation of the immune system. According to the Histiocyte Society’s 2004 guidelines, patients must meet five of eight criteria to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e63edef0a59c8e430221644dd3cec99
https://doi.org/10.22541/au.160091430.00702758
https://doi.org/10.22541/au.160091430.00702758
Autor:
Gunjan M. Modi, Victoria L. Williams, Kristy Flemming, Ricardo Guirola, Cecilia Rosales, Marietta M. DeGuzman
Publikováno v:
Pediatric Dermatology. 29:473-478
We present the case of an 8-year-old girl who presented with distal extremity necrosis of the hands, feet, nose, and ears as an acute manifestation of cutaneous polyarteritis nodosa (CPAN). She was emergently managed with intravenous steroids, nifedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49a5897681ded4cc5e1e1cac70c5d32a
https://doi.org/10.1111/j.1525-1470.2011.01515.x
https://doi.org/10.1111/j.1525-1470.2011.01515.x
Autor:
Ricardo Guirola, Karen W. Eldin, Douglas Moodie, Elijah H. Bolin, Charles D. Fraser, Robert Warren
Publikováno v:
Congenital Heart Disease. 6:630-633
Takayasu arteritis (TA) is a large-vessel arteritis affecting the aorta and its major branches. It is a rare disease in children less than 10 years old, and its diagnosis is frequently delayed, likely because of TA's rarity and nonspecific symptoms e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dab6fea41d72c6be063733f22c37fb9
https://doi.org/10.1111/j.1747-0803.2011.00592.x
https://doi.org/10.1111/j.1747-0803.2011.00592.x
Publikováno v:
Journal of child neurology. 29(1)
Polyarteritis nodosa is a systemic necrotizing vasculitis involving medium-sized muscular arteries. Polyneuropathy is the only neurologic manifestation included in the pediatric classification schema. Central nervous system manifestations include inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aa9338632ddb97552f12fc74f1cba9e
https://pubmed.ncbi.nlm.nih.gov/23155205
https://pubmed.ncbi.nlm.nih.gov/23155205
Autor:
Victoria L, Williams, Ricardo, Guirola, Kristy, Flemming, Gunjan M, Modi, Cecilia, Rosales, Marietta M, DeGuzman
Publikováno v:
Pediatric dermatology. 29(4)
We present the case of an 8-year-old girl who presented with distal extremity necrosis of the hands, feet, nose, and ears as an acute manifestation of cutaneous polyarteritis nodosa (CPAN). She was emergently managed with intravenous steroids, nifedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93dc98a3e781fa63c6325d25b4c0e4b7
https://pubmed.ncbi.nlm.nih.gov/22612230
https://pubmed.ncbi.nlm.nih.gov/22612230
Autor:
Elijah, Bolin, Douglas S, Moodie, Charles D, Fraser, Ricardo, Guirola, Robert, Warren, Karen W, Eldin
Publikováno v:
Congenital heart disease. 6(6)
Takayasu arteritis (TA) is a large-vessel arteritis affecting the aorta and its major branches. It is a rare disease in children less than 10 years old, and its diagnosis is frequently delayed, likely because of TA's rarity and nonspecific symptoms e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15ad7334f854570f12dfc7cea61d0ea7
https://pubmed.ncbi.nlm.nih.gov/22117861
https://pubmed.ncbi.nlm.nih.gov/22117861