Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 1-Nov-2012 | Frasier syndrome: four new cases with unusual presentations | Guaragna, Mara Sanches; Lutaif, Anna Cristina Gervásio de Britto; Bittencourt, Viviane Barros; Piveta, Cristiane Santos Cruz; Soardi, Fernanda Caroline; Castro, Luiz Claudio Gonçalves; Belangero, Vera Maria Santoro; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil; De Mello, Maricilda Palandi | - | Artigo de periódico |
| 1-Nov-2008 | Absence of mutations in Pax6 gene in three cases of Morning Glory syndrome associated with isolated growth hormone deficiency | Guerra-Junior, Gil; Spinola-Castro, Angela Maria; Siviero-Miachon, Adriana A.; Nogueira, Roberto Gomes; Lemos-Marini, Sofia Helena V.; D'Souza-Li, Lilia Freire Rodrigues; Silva, Priscila Cristina da; França, Emerson Salvador S.; Soardi, Fernanda Caroline; Mello, Maricilda Palandi de | - | Artigo de periódico |
| 1-Nov-2008 | Clinical and genetic findings of five patients with WT1-related disorders | Andrade, Juliana Gabriel R. de; Guaragna, Mara Sanches; Soardi, Fernanda Caroline; Guerra-Júnior, Gil; Mello, Maricilda Palandi de; Maciel-Guerra, Andréa Trevas | - | Artigo de periódico |
| 2010 | The Novel Wt1 Gene Mutation P.h377n Associated To Denys-drash Syndrome. | Guaragna, Mara Sanches; Soardi, Fernanda Caroline; Assumpção, Juliana Godoy; Zambaldi, Lílian de Jesus Girotto; Cardinalli, Izilda Aparecida; Yunes, José Andrés; de Mello, Maricilda Palandi; Brandalise, Silvia Regina; Aguiar, Simone dos Santos | - | Artigo de periódico |
| 1-Nov-2010 | Phenotypic variability in a family with x-linked adrenoleukodystrophy caused by the p.Trp132Ter mutation | Soardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Guerra-Júnior, Gil; Lemos-Marini, Sofia Helena Valente de; de Mello, Maricilda Palandi | - | Artigo de periódico |
| 1-Nov-2010 | Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1 | Fabbri, Helena Campos; Mello, Maricilda Palandi de; Soardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Oliveira, Daniel Minutti de; Denardi, Fernanda Canova; Moura-Neto, Arnaldo; Garmes, Heraldo Mendes; Baptista, Maria Tereza Matias; Matos, Patrícia Sabino de; Lemos-Marini, Sofia Helena Valente de; D'Souza-Li, Lilia Freire Rodrigues; Guerra-Júnior, Gil | - | Artigo de periódico |
| 1-Nov-2010 | Structural aspects of the p.P222Q homozygous mutation of HSD3B2 gene in a patient with congenital adrenal hyperplasia | Lusa, Letícia Gori; Lemos-Marini, Sofia Helena Valente de; Soardi, Fernanda Caroline; Ferraz, Lucio Fabio Caldas; Guerra-Júnior, Gil; Mello, Maricilda Palandi de | - | Artigo de periódico |
| 2013 | New Mutation In The Myocilin Gene Segregates With Juvenile-onset Open-angle Glaucoma In A Brazilian Family. | Braghini, Carolina Ayumi; Neshich, Izabella Agostinho Pena; Neshich, Goran; Soardi, Fernanda Caroline; de Mello, Maricilda Palandi; Costa, Vital Paulino; de Vasconcellos, José Paulo Cabral; de Melo, Mônica Barbosa | - | Artigo de periódico |
| 2012 | Frasier Syndrome: Four New Cases With Unusual Presentations. | Guaragna, Mara Sanches; Lutaif, Anna Cristina Gervásio de Britto; Bittencourt, Viviane Barros; Piveta, Cristiane Santos Cruz; Soardi, Fernanda Caroline; Castro, Luiz Claudio Gonçalves; Belangero, Vera Maria Santoro; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil; Mello, Maricilda Palandi De | - | Artigo de periódico |
| 2010 | Structural Aspects Of The P.p222q Homozygous Mutation Of Hsd3b2 Gene In A Patient With Congenital Adrenal Hyperplasia. | Lusa, Letícia Gori; Lemos-Marini, Sofia Helena Valente de; Soardi, Fernanda Caroline; Ferraz, Lucio Fabio Caldas; Guerra-Júnior, Gil; Mello, Maricilda Palandi de | - | Artigo de periódico |
| 2010 | Long-term Follow-up Of An 8-year-old Boy With Insulinoma As The First Manifestation Of A Familial Form Of Multiple Endocrine Neoplasia Type 1. | Fabbri, Helena Campos; Mello, Maricilda Palandi de; Soardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Oliveira, Daniel Minutti de; Denardi, Fernanda Canova; Moura-Neto, Arnaldo; Garmes, Heraldo Mendes; Baptista, Maria Tereza Matias; Matos, Patrícia Sabino de; Lemos-Marini, Sofia Helena Valente de; D'Souza-Li, Lilia Freire Rodrigues; Guerra-Júnior, Gil | - | Artigo de periódico |
| 2010 | Phenotypic Variability In A Family With X-linked Adrenoleukodystrophy Caused By The P.trp132ter Mutation. | Soardi, Fernanda Caroline; Esquiaveto-Aun, Adriana Mangue; Guerra-Júnior, Gil; Lemos-Marini, Sofia Helena Valente de; Mello, Maricilda Palandi de | - | Artigo de periódico |
| 2014 | The Novel P.cys65tyr Mutation In Nr5a1 Gene In Three 46,xy Siblings With Normal Testosterone Levels And Their Mother With Primary Ovarian Insufficiency. | Fabbri, Helena Campos; de Andrade, Juliana Gabriel Ribeiro; Soardi, Fernanda Caroline; de Calais, Flávia Leme; Petroli, Reginaldo José; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil; de Mello, Maricilda Palandi | - | Artigo de periódico |
| 2011 | Molecular Diagnosis Of 5α-reductase Type Ii Deficiency In Brazilian Siblings With 46,xy Disorder Of Sex Development. | Leme de Calais, Flávia Leme; Soardi, Fernanda Caroline; Petroli, Reginaldo José; Lusa, Ana Letícia Gori; de Paiva E Silva, Roberto Benedito; Maciel-Guerra, Andréa Trevas; Guerra-Júnior, Gil; de Mello, Maricilda Palandi | - | Artigo de periódico |
| 2008 | Absence Of Mutations In Pax6 Gene In Three Cases Of Morning Glory Syndrome Associated With Isolated Growth Hormone Deficiency. | Guerra-Junior, Gil; Spinola-Castro, Angela Maria; Siviero-Miachon, Adriana A; Nogueira, Roberto Gomes; Lemos-Marini, Sofia Helena V; D'Souza-Li, Lilia Freire Rodrigues; Silva, Priscila Cristina da; França, Emerson Salvador S; Soardi, Fernanda Caroline; Mello, Maricilda Palandi de | - | Artigo de periódico |
| 2008 | Heterozygosis For Cyp21a2 Mutation Considered As 21-hydroxylase Deficiency In Neonatal Screening. | Soardi, Fernanda Caroline; Lemos-Marini, Sofia Helena V; Coeli, Fernanda Borchers; Maturana, Víctor Gonçalves; Silva, Márcia Duarte Barbosa da; Bernardi, Renan Darin; Justo, Giselle Zenker; de-Mello, Maricilda Palandi | - | Artigo de periódico |
| 1-Nov-2008 | Heterozygosis for CYP21A2 mutation considered as 21-hydroxylase deficiency in neonatal screening | Soardi, Fernanda Caroline; Lemos-Marini, Sofia Helena V.; Coeli, Fernanda Borchers; Maturana, Víctor Gonçalves; Silva, Márcia Duarte Barbosa da; Bernardi, Renan Darin; Justo, Giselle Zenker; de-Mello, Maricilda Palandi | - | Artigo de periódico |
| 2008 | Mutações novas dos genes CYP21A2 e CYP11B1 e suas alferações na atividade enzimatica | Soardi, Fernanda Caroline | Mello, Maricilda Palandi de; Sonati, Maria de Fátima, 1958- | TESE |
| 2015 | Investigation of polymorphisms in pre-eclampsia related genes VEGF and IL1A | Silva, Vanessa Resende Souza; Soardi, Fernanda Caroline; Tanaka, Sarah Cristina Sato Vaz; Silva-Grecco, Roseane Lopes da; Paschoini, Marina Carvalho; Balarin, Marly Aparecida Spadotto | - | Artigo |