Clinical Evaluation of Different Delivery Methods of At-Home Bleaching Gels Composed of 10% Hydrogen Peroxide von Cordeiro, D, Toda, C, Hanan, S, Arnhold, L P, Reis, A, Loguercio, A D, Bandeira, Mf Costa Lima

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Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature von Vasques, Gabriela A, Amano, Naoko, Docko, Ana J, Funari, Mariana F. A, Quedas, Elisangela P. S, Nishi, Mirian Y, Arnhold, Ivo J. P, Hasegawa, Tomonobu, Jorge, Alexander A. L

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Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes von Davis, S.W., Castinetti, F., Carvalho, L.R., Ellsworth, B.S., Potok, M.A., Lyons, R.H., Brinkmeier, M.L., Raetzman, L.T., Carninci, P., Mortensen, A.H., Hayashizaki, Y., Arnhold, I.J.P., Mendonça, B.B., Brue, T., Camper, S.A.

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Mutations of the KISS1 Gene in Disorders of Puberty von Silveira, L. G., Noel, S. D., Silveira-Neto, A. P., Abreu, A. P., Brito, V. N., Santos, M. G., Bianco, S. D. C., Kuohung, W., Xu, S., Gryngarten, M., Escobar, M. E., Arnhold, I. J. P., Mendonca, B. B., Kaiser, U. B., Latronico, A. C.

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Multigene Sequencing Analysis of Children Born Small for Gestational Age With Isolated Short Stature von Freire, Bruna L, Homma, Thais K, Funari, Mariana F A, Lerario, Antônio M, Vasques, Gabriela A, Malaquias, Alexsandra C, Arnhold, Ivo J P, Jorge, Alexander A L

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Acute Myocardial Infarction Reduces Respiration in Rat Cardiac Fibers, despite Adipose Tissue Mesenchymal Stromal Cell Transplant von Lindoso, Rafael S., Vieyra, Adalberto, Galina, Antonio, Goldenberg, Regina C. S., Suhett, Grazielle D., Pimentel, Cibele F., Ferreira, Raphaela P., de Moraes, Alan C. N., de Andrade, Cherley B. V., Christie, Michelle L. A., Martins, Eduarda L., Nguyen, Michelle T., Campos de Carvalho, Antonio C.

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Growth Hormone (GH) Pharmacogenetics: Influence of GH Receptor Exon 3 Retention or Deletion on First-Year Growth Response and Final Height in Patients with Severe GH Deficiency von Jorge, Alexander A. L., Marchisotti, Frederico G., Montenegro, Luciana R., Carvalho, Luciani R., Mendonca, Berenice B., Arnhold, Ivo J. P.

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Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways von Canton, Ana P M, Costa, Sílvia S, Rodrigues, Tatiane C, Bertola, Debora R, Malaquias, Alexsandra C, Correa, Fernanda A, Arnhold, Ivo J P, Rosenberg, Carla, Jorge, Alexander A L

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The phenotypic spectrum associated with OTX2 mutations in humans von Gregory, Louise C, Gergics, Peter, Nakaguma, Marilena, Bando, Hironori, Patti, Giuseppa, McCabe, Mark J, Fang, Qing, Ma, Qianyi, Ozel, Ayse Bilge, Li, Jun Z, Poina, Michele Moreira, Jorge, Alexander A L, Benedetti, Anna F Figueredo, Lerario, Antonio M, Arnhold, Ivo J P, Mendonca, Berenice B, Maghnie, Mohamad, Camper, Sally A, Carvalho, Luciani R S, Dattani, Mehul T

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Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly von França, Marcela M, Jorge, Alexander A. L, Carvalho, Luciani R. S, Costalonga, Everlayny F, Vasques, Gabriela A, Leite, Claudia C, Mendonca, Berenice B, Arnhold, Ivo J. P

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Noonan syndrome associated with growth hormone deficiency with biallelic LZTR1 variants von Nakaguma, Marilena, Jorge, Alexander A.L., Arnhold, Ivo J.P.

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Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders von Vasques, Gabriela A., Arnhold, Ivo J.P., Jorge, Alexander A.L.

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Growth standards of patients with Noonan and Noonan-like syndromes with mutations in the RAS/MAPK pathway von Malaquias, Alexsandra C., Brasil, Amanda S., Pereira, Alexandre C., Arnhold, Ivo J.P., Mendonca, Berenice B., Bertola, Debora R., Jorge, Alexander A.L.

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Role of GLI2 in hypopituitarism phenotype von Arnhold, Ivo J P, França, Marcela M, Carvalho, Luciani R, Mendonca, Berenice B, Jorge, Alexander A L

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High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency von Gergics, Peter, Smith, Cathy, Bando, Hironori, Jorge, Alexander A.L., Rockstroh-Lippold, Denise, Vishnopolska, Sebastian A., Castinetti, Frederic, Maksutova, Mariam, Carvalho, Luciani Renata Silveira, Hoppmann, Julia, Martínez Mayer, Julián, Albarel, Frédérique, Braslavsky, Debora, Keselman, Ana, Bergadá, Ignacio, Martí, Marcelo A., Saveanu, Alexandru, Barlier, Anne, Abou Jamra, Rami, Guo, Michael H., Dauber, Andrew, Nakaguma, Marilena, Mendonca, Berenice B., Jayakody, Sajini N., Ozel, A. Bilge, Fang, Qing, Ma, Qianyi, Li, Jun Z., Brue, Thierry, Pérez Millán, María Ines, Arnhold, Ivo J.P., Pfaeffle, Roland, Kitzman, Jacob O., Camper, Sally A.

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Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability von Dantas, Naiara C B, Funari, Mariana F A, Lerário, Antonio M, Andrade, Nathalia L M, Rezende, Raíssa C, Cellin, Laurana P, Alves, Crésio, Crisostomo, Lindiane G, Arnhold, Ivo J P, Mendonca, Berenice, Scalco, Renata C, Jorge, Alexander A L

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Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single... von Otto, Aline P., França, Marcela M., Correa, Fernanda A., Costalonga, Everlayny F., Leite, Claudia C., Mendonca, Berenice B., Arnhold, Ivo J. P., Carvalho, Luciani R. S., Jorge, Alexander A. L.

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Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery von Correa, Fernanda A., Nakaguma, Marilena, Madeira, João L. O., Nishi, Mirian Y., Abrão, Milena G., Jorge, Alexander A. L., Carvalho, Luciani R., Arnhold, Ivo J. P., Mendonça, Berenice B.

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Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p.Arg511Trp) von Leal, Andrea C., Montenegro, Luciana R., Saito, Renata F., Ribeiro, Tamaya C., Coutinho, Debora C., Mendonca, Berenice B., Arnhold, Ivo J. P., Jorge, Alexander A. L.

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A Bayesian Approach to Diagnose Growth Hormone Deficiency in Children: Insulin-Like Growth Factor Type 1 Is Valuable for Screening and IGF-Binding Protein Type 3 for Confirmation von Inoue-Lima, Thais H., Vasques, Gabriela A., Nakaguma, Marilena, Brito, Luciana Pinto, Mendonça, Berenice B., Arnhold, Ivo J.P., Jorge, Alexander A.L.

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