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38 results

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Page 1
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: bartolotta e. J Clin Endocrinol Metab. 1980 Dec;51(6):1316-24. doi: 10.1210/jcem-51-6-1316. J Clin Endocrinol Metab. 1980. PMID: 6449518
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: bartolotta e. J Clin Endocrinol Metab. 1981 Dec;53(6):1193-8. doi: 10.1210/jcem-53-6-1193. J Clin Endocrinol Metab. 1981. PMID: 6271801
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.
Pollack MS, New MI, O'Neill GJ, Levine LS, Callaway C, Pang S, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, Dupont B. Pollack MS, et al. Among authors: bartolotta e. Hum Genet. 1981;58(3):331-7. doi: 10.1007/BF00294933. Hum Genet. 1981. PMID: 6948766
[Pituitary dwarfism. Evaluation of our cases].
Bartolotta E, Giacomozzi E, Migliori C, Conti S. Bartolotta E, et al. Minerva Med. 1982 May 12;73(20):1421-4. Minerva Med. 1982. PMID: 7078818 Italian. No abstract available.
Pulsatile secretion of thyrotropin in children.
Loche S, Cherubini V, Bartolotta E, Lampis A, Carta D, Tomasi P, Pintor C. Loche S, et al. Among authors: bartolotta e. J Endocrinol Invest. 1994 Mar;17(3):189-93. doi: 10.1007/BF03347715. J Endocrinol Invest. 1994. PMID: 8051341
Antigliadin antibodies at onset of diabetes in children.
Catassi C, Guerrieri A, Bartolotta E, Coppa GV, Giorgi PL. Catassi C, et al. Among authors: bartolotta e. Lancet. 1987 Jul 18;2(8551):158. doi: 10.1016/s0140-6736(87)92357-9. Lancet. 1987. PMID: 2885618 No abstract available.
[Obesity in children].
Giacomozzi E, Bartolotta E, Felici L. Giacomozzi E, et al. Among authors: bartolotta e. Minerva Med. 1982 May 12;73(20):1415-20. Minerva Med. 1982. PMID: 7078817 Italian. No abstract available.
[Down's syndrome. Personal cases and considerations].
Bartolotta E, Baldoni ME, Bruschi R, Dolci AM, Ferrari F, Giacomozzi E, Migliori MV, Giamagli CA. Bartolotta E, et al. Minerva Med. 1978 Nov 24;69(57):3911-6. Minerva Med. 1978. PMID: 153488 Italian. No abstract available.
Glucagon stimulates GH secretion after intramuscular but not intravenous administration. Evidence against the assumption that glucagon per se has a GH-releasing activity.
Ghigo E, Bartolotta E, Imperiale E, Bellone J, Cardinale G, Aimaretti G, Valetto MR, Cherubini V, Maccario M, Cocchi D, et al. Ghigo E, et al. Among authors: bartolotta e. J Endocrinol Invest. 1994 Dec;17(11):849-54. doi: 10.1007/BF03347790. J Endocrinol Invest. 1994. PMID: 7745232 Clinical Trial.
38 results