Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ioana Micle"'
Autor:
Ramona Stroescu, Ioana Micle, Teofana Bizerea, Monica Mărăzan, Maria Puiu, Gabriela Doroş, Otilia Mărginean
Publikováno v:
Romanian Journal of Pediatrics, Vol 63, Iss 3, Pp 331-335 (2014)
Indicele intimǎ medie carotidian (IMc) este un cunoscut marker subclinic pentru aterosclerozǎ. Fenomenul de recuperare nutriţionalǎ la copiii nǎscuţi mici pentru vârsta gestaţionalǎ (SGA) a fost asociat cu obezitate precoce şi cu riscul d
Externí odkaz:
https://doaj.org/article/79aeb23583884d7498cd331f6805f0ba
Autor:
Ramona Stroescu, Ioana Micle, Teofana Bizerea, Monica Marazan, Maria Puiu, Gabriela Doros, Otilia Marginean
Publikováno v:
Romanian Journal of Pediatrics, Vol 63, Iss 3, Pp 270-275 (2014)
The intima media thickness of the common carotid artery (CIMT) is a well-known marker of subclinical atherosclerosis. The “catch-up growth” phenomenon in children born small for gestational age (SGA) has been linked to early onset obesity with th
Externí odkaz:
https://doaj.org/article/d6d0339aa8df4c6e8b566c80391c8774
Publikováno v:
Romanian Journal of Pediatrics, Vol 61, Iss 1, Pp 77-83 (2012)
Introducere. În copilărie, hipoglicemia persistentă are un impact negativ major asupra dezvoltării structurale şi funcţionale a creierului. În perioada de sugar, hipoglicemia poate fi forma de prezentare a defi citului de hormon de creştere
Externí odkaz:
https://doaj.org/article/acdb946a8660497d8b920d05b296e5e2
Autor:
Adela Chiriţă, Ramona Cojocaru, Monica Marazan, Corina Duncescu, Ramona Stroescu, Bogdana Zoica, Ioana Micle
Publikováno v:
Romanian Journal of Pediatrics, Vol 61, Iss 1, Pp 69-76 (2012)
Introducere. Sindromul adrenogenital este o boală genetică care are ca rezultat producţia scăzută de cortizol şi aldosteron. Pacienţii de sex masculin cu sindrom adrenogenital pot prezenta tumori adrenotesticulare. Scop. Discutarea caracteris
Externí odkaz:
https://doaj.org/article/aea03d2831544b8ea72d88ea5275dea9
Publikováno v:
Romanian Journal of Pediatrics, Vol 60, Iss 3, Pp 214-222 (2011)
Pubertatea este un proces biologic ce presupune modifi cări fi zice şi psihologice majore, la fi nele căruia copilul devine adult. Clinic, debutul pubertăţii este anunţat de apariţia caracterelor sexuale secundare ce evoluează specifi c pen
Externí odkaz:
https://doaj.org/article/4195984ffd4a4ec882c898cab3943a49
Publikováno v:
Romanian Journal of Pediatrics, Vol 60, Iss 3, Pp 269-274 (2011)
Introducere: Sindromul HAIR-AN este subfenotip al sindromului ovarelor polichistice şi este caracterizat prin hiperandrogenism (HA), insulinorezistenţă (IR) şi acantozis nigricans (AN), asociate cu obezitate. Nu este o boală rară. Incidenţa a
Externí odkaz:
https://doaj.org/article/4500627b791c431f967884cab5e14947
Publikováno v:
Romanian Journal of Pediatrics, Vol 60, Iss 3, Pp 257-268 (2011)
Introducere: hipertiroidismul neonatal apare la nou-născuţii din mamă cu Graves Basedow, frecvenţa bolii fi ind de 1:70. Scopul lucrării: sublinierea complicaţiilor ce pot să apară la nou-născuţii proveniţi din aceste mame. Material şi
Externí odkaz:
https://doaj.org/article/edb743f5220543b3a04d78d4af1f1e60
Autor:
Mariana Maruşteri, Ioana Micle, Carmen Petrescu, D. Savescu, Ghizela Kanalasz, Mirela Manea, Eleonora Gheoghiu, Simona Cerbu, Dorinela Zaboş, Elena Gamaniuc, D. Mihailov, Gabriela Doro scedil, Gratian Dragoslav, Cristian Negru
Publikováno v:
Posters.
Background and aimsCerebral sinovenous thrombosis (CSVT) are increasingly recognised in children but still underdiagnosed. CSVT in children may be fatal and frequently associated with adverse outcomes.MethodsSeven children diagnosed with CSVT between
Publikováno v:
Obesity Research & Clinical Practice. 8:e592-e598
Summary Introduction The "catch-up growth" phenomenon in children born small for gestational age (SGA) has been linked to early onset obesity with the subsequent emergence of metabolic syndrome (MetS) or its components. It has been postulated that th
Autor:
I. Capalnasan, Ioana Micle
Publikováno v:
Annals of West University of Timisoara: Series of Biology, Vol V-VI, Pp 55-60 (2003)
A case of a female pseudohermaphroditism is presented. The aetiologic frame and genetic counseling indications are based on cytogenetic, biochemical and clinical investigations of the patient and on familial inquiry concerning sibship and pregnancy e