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Clinical Endocrinology|July 30, 2013
Diagnosis and complications of Cushing's disease: gender-related differencesMarialuisa Zilio, Mattia Barbot, Filippo Ceccato, et al.
Neurosurgical Review|June 23, 2019
Perioperative multidisciplinary management of endoscopic transsphenoidal surgery for sellar lesions: practical suggestions from the Padova modelM Barbot, F Ceccato, L Lizzul, et al.
Pituitary|May 30, 2016
Second-line tests in the differential diagnosis of ACTH-dependent Cushing's syndromeMattia Barbot, Laura Trementino, Marialuisa Zilio, et al.
The Journal of Cell Biology|July 14, 1998
Functional specialization of stable and dynamic microtubules in protein traffic in WIF-B cellsC Poüs, K Chabin, A Drechou, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Interest of routine measurement of serum calcitonin: study in a large series of thyroidectomized patients. The French Medullary Study GroupP Niccoli, N Wion-Barbot, P Caron, et al.
Brain Sciences|May 28, 2022
Facial Expression Time Processing in Typical Development and in Patients with Congenital Facial PalsyMauro Belluardo, Elisa De Stefani, Anna Barbot, et al.
Hemoglobin|November 28, 2012
Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six casesCeleste Bento, Ana Catarina Oliveira, Joana Neves, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Revised spectrum of mutations in sarcoglycanopathiesMadiha Trabelsi, Niloufar Kavian, Fatma Daoud, et al.
Archives of Neurology|February 15, 2001
Recessive ataxia with ocular apraxia: review of 22 Portuguese patientsC Barbot, P Coutinho, R Chorão, et al.
British Journal of Haematology|July 23, 1998
Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemiaT J Vulliamy, J S Kaeda, D Ait-Chafa, et al.
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