Search Results - "Della Manna, Thais"

Pitfalls in the diagnosis of insulin autoimmune syndrome (Hirata's disease) in a hypoglycemic child: a case report and review of the literature by Dos Santos, Tiago Jeronimo, Passone, Caroline Gouvêa Buff, Ybarra, Marina, Ito, Simone Sakura, Teles, Milena Gurgel, Manna, Thais Della, Damiani, Durval

“…Background Insulin autoimmune syndrome (IAS) is a rare cause of hyperinsulinemic hypoglycemia (HH) not addressed as a potential differential diagnosis in…”
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COMPLEXITY OF PEDIATRIC CHRONIC DISEASE: CROSS-SECTIONAL STUDY WITH 16,237 PATIENTS FOLLOWED BY MULTIPLE MEDICAL SPECIALTIES by Passone, Caroline Gouveia Buff, Grisi, Sandra Josefina, Farhat, Sylvia Costa, Manna, Thais Della, Pastorino, Antonio Carlos, Alveno, Renata Antunes, Miranda, Caroline Vasconcelos Sá, Waetge, Aurora Rosaria, Cordon, Mariana Nutti, Odone-Filho, Vicente, Tannuri, Uenis, Carvalho, Werther Brunow, Carneiro-Sampaio, Magda, Silva, Clovis Artur

“…To assess demographic data and characteristics of children and adolescents with pediatric chronic diseases (PCD), according to the number of…”
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Translation and validation of Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module) in Brazil-Portuguese language by Garcia, Leila F. dos S., Manna, Thais Della, Passone, Caroline de Gouveia Buff, Oliveira, Lygia Spassapan de

“…The aim of the present study was to create a translated version of the Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module)…”
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Subcutaneous Use of a Fast-Acting Insulin Analog: An alternative treatment for pediatric patients with diabetic ketoacidosis by Della Manna, Thais, Steinmetz, Leandra, Campos, Paula R, Farhat, Sylvia C.L, Schvartsman, Cláudio, Kuperman, Hilton, Setian, Nuvarte, Damiani, Durval

“…OBJECTIVE:--To look for technical simplification and economic efficiency in the treatment of pediatric diabetic ketoacidosis (DKA) with subcutaneous use of the…”
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Economic status and clinical care in young type 1 diabetes patients: a nationwide multicenter study in Brazil by Gomes, Marilia B., de Mattos Matheus, Alessandra Saldanha, Calliari, Luis Eduardo, Luescher, Jorge Luiz, Manna, Thais Della, Savoldelli, Roberta Diaz, Cobas, Roberta A., Coelho, Wellington Siqueira, Tschiedel, Balduino, Ramos, Alberto José, Fonseca, Reine Marie, Araujo, Neuza Braga C., Almeida, Henriqueta Guido, Melo, Naira Horta, Jezini, Debora Laredo, Negrato, Carlos Antonio

“…The aim of this study is to evaluate the influence of economic status on clinical care provided to Brazilian youths with type 1 diabetes in daily practice,…”
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Translation and validation of diabetes self-management profile (DSMP) into Brazilian Portuguese language: first instrument to assess type 1 diabetes self-management in a pediatric population by Passone, Caroline Gouveia Buff, Esteves, Lygia Spassapan Oliveira, Savoldelli, Roberta Dias, Harris, Michael A, Damiani, Durval, Manna, Thais Della

“…To translate and validate the instrument Diabetes Self-Management Profile (DSMP)-Conventional and Flexible Regimens into Brazilian Portuguese language in order…”
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Maturity-Onset Diabetes of the Young (MODY) in Brazil: establishment of a national registry and appraisal of available genetic and clinical data by M.A. Giuffrida, Fernando, Moises, Regina S, Weinert, Leticia S, Calliari, Luis E, Della Manna, Thais, Dotto, Renata P, Franco, Luciana, Caetano, Lilian A, Teles, Milena G, Andrade Lima, Renata, Alves, Crésio, Dib, Sergio A, Silveiro, Sandra P, Dias-da-Silva, Magnus R, Reis ¶, Andre F

“…Highlights • A national registry of MODY cases in Brazil was established. • 311 individuals were assessed, 72 with GCK mutations and 31 with HNF1A mutations. •…”
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Three unreported glucokinase ( GCK ) missense mutations detected in the screening of thirty-two Brazilian kindreds for GCK and HNF1A -MODY by Weinert, Letícia S, Silveiro, Sandra P, Giuffrida, Fernando M.A, Cunha, Vivian T, Bulcão, Caroline, Calliari, Luis Eduardo, Manna, Thais Della, Kunii, Ilda S, Dotto, Renata P, Dias-da-Silva, Magnus R, Reis, André F

“…Highlights • Thirty-two Brazilian families with MODY phenotype have been studied. • Mutations in HNF1A and glucokinase ( GCK ) have been assessed. • Eight…”
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A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian families by Giuffrida, Fernando M.A, Calliari, Luis Eduardo, Manna, Thais Della, Ferreira, João Guimarães, Saddi-Rosa, Pedro, Kunii, Ilda S, Furuzawa, Gilberto K, Dias-da-Silva, Magnus R, Reis, Andre F

“…Abstract Six Brazilian families with mild familial hyperglycaemia have been screened for glucokinase ( GCK ) mutations. All had mutations that co-segregated…”
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Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome by Gasparin, Maria Regina R, Crispim, Felipe, Paula, Sílvia L, Freire, Maria Beatriz S, Dalbosco, Ivaldir S, Manna, Thais Della, Salles, João Eduardo N, Gasparin, Fábio, Guedes, Aléxis, Marcantonio, João M, Gambini, Márcio, Salim, Camila P, Moisés, Regina S

“…ObjectiveWolfram syndrome (WS) is a rare, progressive, neurodegenerative disorder with an autosomal recessive pattern of inheritance. The gene for WS, WFS1,…”
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Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome by Reis, André F, Kannengiesser, Caroline, Jennane, Farida, Manna, Thais Della, Cheurfa, Nadir, Oudin, Claire, Savoldelli, Roberta Diaz, Oliveira, Carolina, Grandchamp, Bernard, Kok, Fernando, Velho, Gilberto

“…Reis AF, Kannengiesser C, Jennane F, Manna TD, Cheurfa N, Oudin C, Savoldelli RD, Oliveira C, Grandchamp B, Kok F, Velho G. Two novel mutations in the EIF2AK3…”
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Health-related quality of life in patients with type 1 diabetes mellitus in the different geographical regions of Brazil: data from the Brazilian Type 1 Diabetes Study Group by Felício, João Soares, de Souza, Ana Carolina Contente Braga, Koury, Camila Cavalcante, Neto, João Felício Abrahão, Miléo, Karem Barbosa, Santos, Flávia Marques, Motta, Ana Regina Bastos, Silva, Denisson Dias, Arbage, Thaís Pontes, Carvalho, Carolina Tavares, de Rider Brito, Hana Andrade, Yamada, Elizabeth Sumi, Cobas, Roberta Arnoldi, Matheus, Alessandra, Tannus, Lucianne, Palma, Catia Cristina Sousa, Japiassu, Leticia, Carneiro, João Regis Ivar, Rodacki, Melanie, Zajdenverg, Lenita, de Araújo, Neuza Braga Campos, de Menezes Cordeiro, Marilena, Luescher, Jorge Luiz, Berardo, Renata Szundy, Nery, Marcia, Cani, Catarina, do Carmo Arruda Marques, Maria, Calliari, Luiz Eduardo, de Noronha, Renata Maria, Manna, Thais Della, Savoldelli, Roberta, Penha, Fernanda Garcia, Foss, Milton Cesar, Foss-Freitas, Maria Cristina, Pires, Antonio Carlos, Robles, Fernando Cesar, Negrato, Carlos Antonio, de Fatima Guedes, Maria, Dib, Sergio Atala, Dualib, Patricia, da Silva, Saulo Cavalcanti, Sepúlveda, Janice, Sampaio, Emerson, Rea, Rosangela Roginski, de Almeida Faria, Ana Cristina Ravazzani, Tschiedel, Balduino, Lavigne, Suzana, Cardozo, Gustavo Adolfo, Azevedo, Mirela, Canani, Luis Henrique, Zucatti, Alessandra Teixeira, Coral, Marisa Helena Cesar, Pereira, Daniela Aline, de Araujo, Luiz Antonio, Pedrosa, Hermelinda Cordeiro, Tolentino, Monica, Prado, Flaviene Alves, Rassi, Nelson, de Araujo, Leticia Bretones, Fonseca, Reine Marie Chaves, Guedes, Alexis Dourado, de Mattos, Odelisa Silva, Faria, Manuel, Azulay, Rossana, E Forti, Adriana Costa, Façanha, Cristina Figueiredo Sampaio, Junior, Renan Montenegro, Montenegro, Ana Paula, Melo, Naira Horta, Rezende, Karla Freire, Ramos, Alberto, Jezini, Deborah Laredo, Gomes, Marilia Brito

“…In type 1 diabetes mellitus (T1DM) management, enhancing health-related quality of life (HRQoL) is as important as good metabolic control and prevention of…”
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Not every diabetic child has type 1 diabetes mellitus by Della Manna, Thais

“…Although it is type 1 diabetes mellitus of autoimmune origin that is most prevalent in childhood and adolescence, other forms of diabetes can also affect this…”
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Efficacy of photographic educational materials for carbohydrate counting training of adolescents with diabetes mellitus by Servilha Gandolfo, Adriana, Vasconcelos Bastos, Débora, Jabur Makluf, Bruna Abreu, de Cassya Lopes Neri, Lenycia, Diaz Savoldelli, Roberta, Della Manna, Thais, Damiani, Durval, Archanjo Ferraro, Alexandre

“…Carbohydrate counting (CHC) is ack - nowledged by the American Diabetes Association (ADA) as an important tool. To assess the efficacy of photographic…”
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Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells by Lovisolo, Silvana M., MendonÇa, Berenice B., Pinto, Emilia M., Manna, Thais Della, Saldiva, Paulo Hilário N., Zerbini, Maria Cláudia N.

“…Congenital hyperinsulinism (CHI) is a rare pancreatic β-cell disease of neonates, characterized by inappropriate insulin secretion with severe persistent…”
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Severe Hypercalcemia in a 9-Year-Old Brazilian Girl Due to a Novel Inactivating Mutation of the Calcium-Sensing Receptor by Miyashiro, Kozue, Kunii, Ilda, Manna, Thais Della, de Menezes Filho, Hamilton C., Damiani, Durval, Setian, Nuvarte, Hauache, Omar M.

“…Familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) are consequent to inactivating mutations of the calcium-sensing…”
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Home blood glucose monitoring in type 1 diabetes mellitus by Grossi, Sonia Aurora Alves, Lottenberg, Simão Augusto, Lottenberg, Ana Maria, Della Manna, Thaís, Kuperman, Hilton

“…To determine which of two simplified blood glucose monitoring schemes promotes better metabolic control in type 1 diabetic patients during 12 months of…”
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Subcutaneous Use of a Fast-Acting Insulin Analog by Della Manna, Thais, Steinmetz, Leandra, Campos, Paula R., Farhat, Sylvia C.L., Schvartsman, Cláudio, Kuperman, Hilton, Setian, Nuvarte, Damiani, Durval

“…Subcutaneous Use of a Fast-Acting Insulin Analog An alternative treatment for pediatric patients with diabetic ketoacidosis Thais Della Manna , MD 1 , Leandra…”
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Precocious puberty: an endocrine manifestation in congenital toxoplasmosis by Setian, Nuvarte, Andrade, Regina S F, Kuperman, Hilton, Manna, Thais Della, Dichtchekenian, Vaê, Damiani, Durval

“…We reviewed retrospectively seven children with congenital toxoplasmosis and precocious puberty. All seven showed very high levels of LH (25.2-155.0 IU/ml) and…”
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CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency by WITCHEL, S. F, SMITH, R, CRIVELLARO, C. E, DELLA MANNA, T, DICHTCHEKENIAN, V, SETIAN, N, DAMIANI, D

“…Congenital adrenal hyperplasia caused by 21-hydroxylase deficiency is a common autosomal recessive disorder resulting from mutations in the 21-hydroxylase…”
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