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Mostrati risultati da 1 a 20 di 234
Titolo Data di pubblicazione Autore(i) File
Final stature in a patient with growth hormone deficiency (GHD) type 1A treated with Recombinated Human Insulin-Growth Factor (IGF) 1-gen-2000 Messina, Maria Francesca; Wasniewska, Malgorzata Gabriela; De Luca, Fa; Valenzise, Mariella; Lombardo, Fortunato; DE LUCA, Filippo
Nefrite interstiziale acuta 1-gen-2000 Ruggeri, Caterina; Valenzise, Mariella; M., Rosano; T., Sirchia
Infezioni respiratorie in età pediatrica : ruoli del mycoplasma e della chlamydia nella nostra esperienza 1-gen-2000 Ruggeri, Caterina; L., Mostaccio; T., Sirchia; Valenzise, Mariella
Aldosterone syndrome deficiency type I with non documentations in the CYP 11 B2 gene 1-gen-2000 Wasniewska, Malgorzata Gabriela; DE LUCA, F. R.; Valenzise, Mariella; Lombardo, Fortunato; DE LUCA, Filippo
Acute interstitial nephritis.A cause of inflammatory renal glycosuria 1-gen-2000 Ruggeri, Caterina; Valenzise, Mariella; Rosano, M; Sirchia, T.
Birth weight influences long-term catch-up growth and height prognosis of GH-deficient children treated before the age of 2 years 1-gen-2000 Wasniewska, Malgorzata Gabriela; Arrigo, Teresa; Mariangela, Cisternino; DE LUCA, Francesco 57; Lucia, Ghizzoni; Mohamad, Maghnie; Valenzise, Mariella; DE LUCA, Filippo
Birth weight influences long-term catch-up growth and height prognosis of GH-deficient children treated before the age of 2 years 1-gen-2000 Wasniewska, Malgorzata Gabriela; Arrigo, Teresa; Cisternino, M; DE LUCA, Filippo; Ghizzoni, L; Maghnie, M; Valenzise, Mariella; DE LUCA, F.
Ascite tubercolare: descrizione di un caso in età pediatrica 1-gen-2001 Ruggeri, Caterina; Tulino, V.; Valenzise, Mariella; Visalli, Carmela; Zimbaro, Giovanni
A novel frameshift mutation of the DAX-1 gene in a boy with Xlinked adrenal hypoplasia congenita and no early impairement of the hypothalamus-pituitary-gonadal axis 1-gen-2001 Wasniewska, Malgorzata Gabriela; DE LUCA, Filippo; Lombardo, Fortunato; Messina, Maria Francesca; Valenzise, Mariella; Lasco, A; Arrigo, Teresa
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene 1-gen-2001 Wasniewska, Malgorzata Gabriela; DE LUCA, Filippo; Valenzise, Mariella; Lombardo, Fortunato; DE LUCA, F.
Final height in isolated GH deficiency type 1A: effects of 5- year treatment with IGF-I 1-gen-2001 MESSINA MF; DE LUCA F.; WASNIEWSKA M; VALENZISE M; LOMBARDO F; GHIZZONI L
Hearing loss in congenital hypothalamic hypothyroidism : a wide therapeutic window 1-gen-2002 Wasniewska, Malgorzata Gabriela; DE LUCA, Filippo; Messina, Maria Francesca; Salzano, Giuseppina; Valenzise, Mariella; Rosano, M.
Circumferential ringed creases and hypertricosis at birth 1-gen-2002 Valenzise, Mariella; Gb, Ferrero; L., Sorasio; M., Silengo
Two-year prospective evaluation of the factors affecting honeymoon frequency and duration in children with insulin dependent diabetes mellitus: The key-role of age at diagnosis 1-gen-2002 Lombardo, Fortunato; Valenzise, Mariella; Wasniewska, Malgorzata Gabriela; Messina, Maria Francesca; Ruggeri, Caterina; Arrigo, Teresa; DE LUCA, Filippo
Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window 1-gen-2002 Wasniewska, Malgorzata Gabriela; DE LUCA, Filippo; Siclari, S; Salzano, Giuseppina; Messina, Maria Francesca; Lombardo, Fortunato; Valenzise, Mariella; Ruggeri, Caterina; Arrigo, Teresa
Catechol-o-methyltransferase inhibition in the treatment of tetrahydrobiopterin deficiency 1-gen-2002 A., Ponzone; S., Baglieri; G., Battistoni; A., Peduto; C., Giovannozzi; Valenzise, Mariella; S., Ferraris; A., Martini; M., Spada
Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4 year-old boy. ) 1-gen-2002 Valenzise, Mariella; G. B., Ferrero; M. T., Tosi; S., Ferraris; M., Silengo
A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Clin Dysmorph 1-gen-2002 M., Silengo; L., Barberis; Gb, Ferrero; L., Sorasio; Valenzise, Mariella
Three-year prospective evaluation of glucose tolerance, beta- cell function and peripheral insulin sensitivity in non- diabetic patients with thalassemia major 1-gen-2002 Messina, Maria Francesca; Lombardo, Fortunato; Meo, Anna; Miceli, M; Wasniewska, Malgorzata Gabriela; Valenzise, Mariella; Ruggeri, Caterina; Arrigo, Teresa; DE LUCA, Filippo
The hair as a diagnostic tool in dysmorphology. Clin Genet 1-gen-2002 M., Silengo; Valenzise, Mariella; L., Sorasio; Gb, Ferrero
Mostrati risultati da 1 a 20 di 234
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