Maricilda Palandi de Mello

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Gil Guerra-JuniorUNICAMPDirección de correo verificada de fcm.unicamp.br
Andréa Trevas Maciel GuerraProfessora titular do Depto. de Genética Medica, FCM - UnicampDirección de correo verificada de fcm.unicamp.br
Sofia Helena Valente de Lemos MariniProfessora do Departamento de Pediatria, FCM UnicampDirección de correo verificada de hc.unicamp.br
Antonia Paula Marques de FariaProfessor Associado, Departamento de Genética Médica, FCM-UNICAMPDirección de correo verificada de fcm.unicamp.br
Dra. Juliana Gabriel Ribeiro de AndradeCoordenadora pedagógica da Tribu EducationDirección de correo verificada de tribusaude.com
margaret de castroSchool of Medicine of Ribeirao Preto - University of Sao PauloDirección de correo verificada de fmrp.usp.br
Reginaldo PetroliUniversidade Federal de AlagoasDirección de correo verificada de famed.ufal.br
Lilia D'Souza-LiAssistant Professor fo Pediatrics, University of CampinasDirección de correo verificada de fcm.unicamp.br
Berenice Bilharinho de MendonçaFaculdade de Medicina da Universidade de São PauloDirección de correo verificada de usp.br
Olaf HiortUniversity of LuebeckDirección de correo verificada de uksh.de
Ezequiel Moreira GonçalvesPós doutorando da Faculdade de Ciências Médicas, UNICAMPDirección de correo verificada de pesquisador.cnpq.br
Leticia Esposito Sewaybricker, MD PhDUniversity of Washington, Seattle, USADirección de correo verificada de uw.edu
Társis Paiva VieiraUniversity of CampinasDirección de correo verificada de fcm.unicamp.br
Tania Aparecida Sartori Sanchez Bac...Professora Associada da Faculdade de Medicina da Universidade de São PauloDirección de correo verificada de hcnet.usp.br
Paulo DalgalarrondoProfessor of Psychiatry, University of CampinasDirección de correo verificada de fcm.unicamp.br
Luciana Campos PaulinoUniversidade Federal do ABCDirección de correo verificada de ufabc.edu.br
Lucio Fabio Caldas FerrazProfessor of Genetics and Molecular BiologyDirección de correo verificada de usf.edu.br
Amilton Santos Júniorpsiquiatra unicampDirección de correo verificada de fcm.unicamp.br
Eloisa HRV CeleriProfessora do Departamento de Psiquiatria da UnicampDirección de correo verificada de fcm.unicamp.br
Vera Lúcia Gil-da-silva-LopesLivre Docente em Genética Clínica na Universidade Estadual de CampinasDirección de correo verificada de fcm.unicamp.br

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Maricilda Palandi de Mello

Universidade Estadual de Campinas

Dirección de correo verificada de unicamp.br

Genética Molecular Humana


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
Novel mutations affecting SRY DNA-binding activity: the HMG box N65H associated with 46, XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable … J Assumpção, C Benedetti, A Maciel-Guerra, G Guerra, M Baptista, ... Journal of Molecular Medicine 80, 782-790, 2002	80	2002
Inhibition of CYP21A2 enzyme activity caused by novel missense mutations identified in Brazilian and Scandinavian patients FC Soardi, M Barbaro, IF Lau, SHV Lemos-Marini, MTM Baptista, ... The Journal of Clinical Endocrinology & Metabolism 93 (6), 2416-2420, 2008	72	2008
Mutation update for the NR5A1 gene involved in DSD and infertility H Fabbri‐Scallet, LM de Sousa, AT Maciel‐Guerra, G Guerra‐Júnior, ... Human mutation 41 (1), 58-68, 2020	71	2020
Identification of new world Leishmania using ribosomal gene spacer probes P Guevara, G Alonso, JF da Silveira, M de Mello, JV Scorza, N Añez, ... Molecular and biochemical parasitology 56 (1), 15-26, 1992	70	1992
Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21‐hydroxylase deficiency LC Paulino, M Araujo, G Guerra Jr, S Marini, MP De Mello Acta Paediatrica 88 (3), 275-283, 1999	69	1999
Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency. M De-Araujo, MR Sanches, LA Suzuki, G Guerra Jr, SB Farah, ... Brazilian Journal of Medical and Biological Research= Revista Brasileira de …, 1996	64	1996
XX Maleness and XX True Hermaphroditism in SRY-Negative Monozygotic Twins: Additional Evidence for a Common Origin AT Maciel-Guerra, MP de Mello, FB Coeli, ML Ribeiro, ML Miranda, ... The Journal of Clinical Endocrinology & Metabolism 93 (2), 339-343, 2008	63	2008
Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia N Torres, MP Mello, CMR Germano, LLK Elias, AC Moreira, M Castro Brazilian journal of medical and biological research 36, 1311-1318, 2003	62	2003
Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density PO de Almeida Freire, SHV de Lemos-Marini, AT Maciel-Guerra, ... Journal of Bone and Mineral Metabolism 21, 396-401, 2003	58	2003
Excited indole-3-aldehyde from the peroxidase-catalyzed aerobic oxidation of indole-3-acetic acid. Reaction with and energy transfer to transfer ribonucleic acid MP De Mello, SM De Toledo, M Haun, G Cilento, N Duran Biochemistry 19 (23), 5270-5275, 1980	57	1980
Complete gonadal dysgenesis in clinical practice: the 46, XY karyotype accounts for more than one third of cases VBC Rocha, G Guerra-Júnior, AP Marques-de-Faria, MP de Mello, ... Fertility and sterility 96 (6), 1431-1434, 2011	54	2011
Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency MG Santos, AZ Machado, CN Martins, S Domenice, EMF Costa, MY Nishi, ... BioMed research international 2014, 2014	51	2014
Differential gene expression in response to copper in *Acidithiobacillus ferrooxidans* analyzed by RNA arbitrarily primed polymerase chain reaction LC Paulino, MP de Mello, LMM Ottoboni Electrophoresis 23 (4), 520-527, 2002	47	2002
Screening of Y chromosome microdeletions in 46, XY partial gonadal dysgenesis and in patients with a 45, X/46, XY karyotype or its variants AP dos Santos, JG Ribeiro Andrade, CSC Piveta, J de Paulo, ... BMC Medical Genetics 14, 1-11, 2013	42	2013
OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences BA Barros, SG Moraes, FB Coeli, JG Assumpção, MP De Mello, ... Human reproduction 26 (12), 3450-3455, 2011	42	2011
H28+ C insertion in the CYP21 gene: a novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency IF Lau, FC Soardi, SHV Lemos-Marini, G Guerra Jr, MTM Baptista, ... The Journal of Clinical Endocrinology & Metabolism 86 (12), 5877-5880, 2001	42	2001
Iron‐regulated proteins in *Phanerochaete chrysosporium* and *Lentinula edodes:* Differential analysis by sodium dodecyl sulfate polyacrylamide gel … ML Hernández‐Macedo, A Ferraz, J Rodríguez, LMM Ottoboni, ... Electrophoresis 23 (4), 655-661, 2002	40	2002
408 cases of genital ambiguity followed by single multidisciplinary team during 23 years: etiologic diagnosis and sex of rearing GB De Paula, BA Barros, S Carpini, BJ Tincani, TN Mazzola, ... International journal of endocrinology 2016, 2016	39	2016
Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5α-Reductase Type 2 Deficiency NN Veiga-Junior, PAR Medaets, RJ Petroli, FL Calais, MP de Mello, ... International Journal of Endocrinology 2012, 2012	39	2012
Novel Mutations in CYP11B1 Gene Leading to 11β-Hydroxylase Deficiency in Brazilian Patients FC Soardi, JY Penachioni, GZ Justo, TASS Bachega, M Inacio, ... The Journal of Clinical Endocrinology & Metabolism 94 (9), 3481-3485, 2009	37	2009

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