Anthropometric evaluation of children with SHOX mutations can be used as indication for genetic studies in children of short stature

Por Jorge, Alexander A L, Arnhold, Ivo J P
Publicado em 2007

Increased Transactivation Associated with SOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism

Por Alatzoglou, Kyriaki S., Kelberman, Daniel, Cowell, Christopher T., Palmer, Rodger, Arnhold, Ivo J. P., Melo, Maria E., Schnabel, Dirk, Grueters, Annette, Dattani, Mehul T.
Publicado no Mol Endocrinol (2011)

A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

Por Carvalho, Luciani R., Woods, Kathryn S., Mendonca, Berenice B., Marcal, Nathalie, Zamparini, Andrea L., Stifani, Stefano, Brickman, Joshua M., Arnhold, Ivo J.P., Dattani, Mehul T.
Publicado em 2003

PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation

Por Araujo, Ricardo V, Chang, Claudia V, Cescato, Valter A. S., Fragoso, Maria Candida B. V., Bronstein, Marcello D, Mendonca, Berenice B, Arnhold, Ivo J. P., Carvalho, Luciani R S
Publicado em 2013

Effectiveness of the Combined Recombinant Human Growth Hormone and Gonadotropin-Releasing Hormone Analog Therapy in Pubertal Patients with Short Stature due to SHOX Deficiency

Por Scalco, Renata C., Melo, Suzana S. J., Pugliese-Pires, Patricia N., Funari, Mariana F. A., Nishi, Mirian Y., Arnhold, Ivo J. P., Mendonca, Berenice B., Jorge, Alexander A. L.
Publicado em 2010

HESX1 Mutations in Patients with Congenital Hypopituitarism: Variable Phenotypes with the Same Genotype

Por Fang, Qing, Figueredo Benedetti, Anna Flavia, Ma, Qianyi, Gregory, Louise, Li, Jun Z., Dattani, Mehul, Sadeghi-Nejad, Abdollah, Arnhold, Ivo J.P., de Mendonça, Berenice Bilharinho, Camper, Sally A., Carvalho, Luciani R.
Publicado no Clin Endocrinol (Oxf) (2016)

Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age

Por Coletta, Rocio R D, Jorge, Alexander A L, D' Alva, Catarina Brasil, Pinto, Emília M, Billerbeck, Ana Elisa C, Pachi, Paulo R, Longui, Carlos A, Garcia, Ricardo M, Boguszewski, Margaret, Arnhold, Ivo J P, Mendonca, Berenice B, Costa, Elaine M F
Publicado em 2013

Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies

Por Correa, Fernanda A., Bianchi, Paulo H. M., Franca, Marcela M., Otto, Aline P., Rodrigues, Rodrigo J. M., Ejzenberg, Dani, Serafini, Paulo C., Baracat, Edmundo Chada, Francisco, Rossana P. V., Brito, Vinicius N., Arnhold, Ivo J. P., Mendonca, Berenice B., Carvalho, Luciani R.
Publicado no J Endocr Soc (2017)

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies

Por Correa, Fernanda A, Trarbach, Ericka B, Tusset, Cintia, Latronico, Ana Claudia, Montenegro, Luciana R, Carvalho, Luciani R, Franca, Marcela M, Otto, Aline P, Costalonga, Everlayny F, Brito, Vinicius N, Abreu, Ana Paula, Nishi, Mirian Y, Jorge, Alexander A L, Arnhold, Ivo J P, Sidis, Yisrael, Pitteloud, Nelly, Mendonca, Berenice B
Publicado no Endocr Connect (2015)

Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3

Por Macedo, Delanie B., Abreu, Ana Paula, Reis, Ana Claudia S., Montenegro, Luciana R., Dauber, Andrew, Beneduzzi, Daiane, Cukier, Priscilla, Silveira, Leticia F. G., Teles, Milena G., Carroll, Rona S., Junior, Gil Guerra, Filho, Guilherme Guaragna, Gucev, Zoran, Arnhold, Ivo J. P., de Castro, Margaret, Moreira, Ayrton C., Martinelli, Carlos Eduardo, Hirschhorn, Joel N., Mendonca, Berenice B., Brito, Vinicius N., Antonini, Sonir R., Kaiser, Ursula B., Latronico, Ana Claudia
Publicado em 2014