BARP, LORELLA
BARP, LORELLA
Alma Mater Studiorum Universita' di Bologna
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia
2005 M. Bal;L. Barp;A. Cassio;L. Baldazzi;S. Salardi;L. Lugaresi;A. Cicognani
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene
2005 L. Baldazzi; M. Barbaro; A. Balsamo ;S. Menabò; L. Barp;N. Greggio; L. Iughetti; L. Garavelli; G. Cangemi; A. Antelli; A. Cicognani
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects.
2005 Nicoletti A; Baldazzi L; Balsamo A; Barp L; Pirazzoli P; Gennari M; Radetti G; Cacciari E; Cicognani A.
Height outcome and pubertal development in CYP21 genotyped CAH male patients
2004 A.Balsamo; L.Baldazzi; L.Barp; F.Baronio; M.Gennari; C.Retetangos; A.Cassio; A.Cicognani; E.Cacciari.
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism
2004 A. Antelli; L. Baldazzi; L. Barp; S. Menabò; M. Gennari; A. Cassio; A. Cicognani; E. Cacciari
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia | M. Bal;L. Barp;A. Cassio;L. Baldazzi;S. Salardi;L. Lugaresi;A. Cicognani | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene |
L. Baldazzi; M. Barbaro; A. Balsamo ;S. Menabò; L. Barp;N. Greggio; L. Iughetti; L. Garavelli; G.... Cangemi; A. Antelli; A. Cicognani |
2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. | Nicoletti A; Baldazzi L; Balsamo A; Barp L; Pirazzoli P; Gennari M; Radetti G; Cacciari E; Cicogn...ani A. | 2005-01-01 | CLINICAL ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
| Height outcome and pubertal development in CYP21 genotyped CAH male patients | A.Balsamo; L.Baldazzi; L.Barp; F.Baronio; M.Gennari; C.Retetangos; A.Cassio; A.Cicognani; E.Cacci...ari. | 2004-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism |
A. Antelli; L. Baldazzi; L. Barp; S. Menabò; M. Gennari; A. Cassio; A. Cicognani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |