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Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia.
Published in:
European Journal of Neurology, 2011, v. 18, n. 1, p. 150, doi. 10.1111/j.1468-1331.2010.03102.x
By:
- Battini, R.;
- Fogli, A.;
- Borghetti, D.;
- Michelucci, A.;
- Perazza, S.;
- Baldinotti, F.;
- Conidi, M. E.;
- Ferreri, M. I.;
- Simi, P.;
- Cioni, G.
Publication type:
Article
A Girl with Tomboy Behavior: Lesson from Misdiagnosis in a Baby with Ambiguous Genitalia.
Published in:
Sexual Development, 2010, v. 4, n. 3, p. 150, doi. 10.1159/000273265
By:
- Dati, E.;
- Baldinotti, F.;
- Conidi, M.E.;
- Simi, P.;
- Baroncelli, G.I.;
- Bertelloni, S.
Publication type:
Article
Body Composition and Metabolic Profile in Women with Complete Androgen Insensitivity Syndrome.
Published in:
Sexual Development, 2009, v. 3, n. 4, p. 188, doi. 10.1159/000228719
By:
- Dati, E.;
- Baroncelli, G.I.;
- Mora, S.;
- Russo, G.;
- Baldinotti, F.;
- Parrini, D.;
- Erba, P.;
- Simi, P.;
- Bertelloni, S.
Publication type:
Article
Early Diagnosis of 5α-Reductase Deficiency in Newborns.
Published in:
Sexual Development, 2007, v. 1, n. 3, p. 147, doi. 10.1159/000102103
By:
- Bertelloni, S.;
- Scaramuzzo, R.T.;
- Parrini, D.;
- Baldinotti, F.;
- Tumini, S.;
- Ghirri, P.
Publication type:
Article
P15.01: Surface rendering of external genitalia in fetus at 32 weeks of gestation affected by Partial Androgen Insensitivity Syndrome (PAIS).
Published in:
Ultrasound in Obstetrics & Gynecology, 2009, v. 34, n. S1, p. 232, doi. 10.1002/uog.7201
By:
- Latella, S.;
- Fenu, V.;
- Ceccarelli, P.;
- Baldinotti, F.;
- Iughetti, L.;
- Volpe, A.;
- Mazza, V.
Publication type:
Article
Phenotypic characterization of c.379A > G GJB1 mutation in a Charcot-Marie-Tooth female patient.
Published in:
2023
By:
- Merico, E.;
- Schirinzi, E.;
- Baldinotti, F.;
- Govoni, A.;
- Siciliano, G.
Publication type:
Letter
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey.
Published in:
Prenatal Diagnosis, 2004, v. 24, n. 8, p. 647, doi. 10.1002/pd.962
By:
- Sensi, A.;
- Cavani, S.;
- Villa, N.;
- Pomponi, M. G.;
- Fogli, A.;
- Gualandi, F.;
- Grasso, M.;
- Sala, E.;
- Pietrobono, R.;
- Baldinotti, F.;
- Savin, E.;
- Ferlini, A.;
- Cecconi, M.;
- Rossi, S.;
- Gallone, S.;
- Bellini, C.;
- Neri, G.;
- Martinoli, E.;
- Simi, P.;
- Dalprà, L.
Publication type:
Article

Found: 7

Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia.

A Girl with Tomboy Behavior: Lesson from Misdiagnosis in a Baby with Ambiguous Genitalia.

Body Composition and Metabolic Profile in Women with Complete Androgen Insensitivity Syndrome.

Early Diagnosis of 5α-Reductase Deficiency in Newborns.

P15.01: Surface rendering of external genitalia in fetus at 32 weeks of gestation affected by Partial Androgen Insensitivity Syndrome (PAIS).

Phenotypic characterization of c.379A > G GJB1 mutation in a Charcot-Marie-Tooth female patient.

Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey.