Search results for "38"
showing 10 items of 1730 documents
Tubulointerstitial nephritis and uveitis syndrome post-COVID-19
2023
Pelvic magnetic resonance imaging in Turner syndrome.
2012
Background: Adolescents with Turner Syndrome (TS) live a difficulty related to the prospective to have spontaneous pubertal development and menarche as well as to their future fertility. These questions have relevant psychological-therapeutic implications on clinical and endocrine follow-up and represent critical points in the TS management. Some patients have spontaneous menarche and do not need estroprogestinic replacement in the first years of adolescence. This evolution is not always predictable on the basis of hormonal pattern and echographic imaging, while it is described in patients with mosaicism. Methods: We studied 17 patients with TS, age: 9-16 years, caryotype 45,X in 9 patients…
Trattamento delle piastrinopenie: esperienza annuale
2010
La porpora di Seidlmayer: descrizione di cinque casi
2014
Studio dei potenziali evocati uditivi e visivi nella malattia di Kawasaki: markers di vasculite e conferma diagnostica
2012
"Un mare di bambini": progetto pilota condiviso LNI-SIP
2014
Congenital malformations.
2012
Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or during the intrauterine life. Their global birth prevalence is about 2–3%. Both genetic and environmental factors, as well as their combination in a multifactorial contest, may induce congenital defects. Congenital malformations may be classi- fied on the basis of clinical, etiologic as well as pathogenetic criteria. Relevant diagnostic and therapeutic tools have been progressively improving in the last decades, contributing to a better identification and a reduction of long-term morbidity and mortality of these patients. A correct identification of a congen- ita…
RABDOMIOLISI IN CORSO DI INFEZIONE DA VIRUS PARAINFLUENZALE TRATTATA CON PARACETAMOLO
2009
RACHITISMO VITAMINA-D RESISTENTE DA MUTAZIONE DEL RECETTORE DELLA VITAMINA D: VARIABILITÀ FENOTIPICA IN DUE SORELLE
2017
PRESENTAZIONE DEL CASO, STORIA CLINICA E SINTOMATOLOGIA Il rachitismo vitamina-D resistente (HVDRR), è una patologia a trasmissione autosomica recessiva dovuta a mutazione del gene del recettore per la vitamina D (VDR). L’esordio del rachitismo è precoce e si può associare alopecia. Descriviamo il caso di due sorelle con HVDRR, la loro presentazione clinica e la risposta alla terapia. La primogenita in atto ha 4 anni di età, una ipocalcemia severa e resistente, con scarsa risposta al calcio per via orale somministrato ad alte dosi, ha avuto necessità -nel primo anno di vita- di somministrazione endovenosa di calcio per diversi mesi. La diagnosi è stata posta per l’insorgenza, in assenza di …
RHEUMATHOLOGIC DISEASES IN ADOLESCENCE: PSYCHOLOGICAL PROFILE OF A DIFFICULT AGE
2015
Background: Chronic disease significantly interfere with the quality of life at every age, expecially in a period of life characterized by the need to assume a role in the society and the research of a specific identity. The personal image is often destroyed by the disease, the long term sequelae of pharmacological treatment. Adolescents are frequently obligated to quit many possibilities of experience with peers. Objectives: We realized a plurispecialistic approach to adolescents with rheumatologic diseases, with the figures of neuropsychiatric, psychologists, rheumatologists, endocrinologists, to give an answer to the complex requests of these patients. Methods: We evaluated 20 patients w…