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Lucilene Arilho Ribeiro

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Magnetic Resonance Imaging

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Brazil

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Publications

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Lucilene Arilho Ribeiro; Claudia Danielli Pereira Bertolacini; Rodrigo Gonçalves Quiezi; Antonio Richieri-Costa
A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis.
Lucilene Arilho Ribeiro; Rodrigo Gonçalves Quiezi; Adriana Nascimento; Claudia Pereira Bertolacini; Antonio Richieri-Costa
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patients.
Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in Brazil.

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All Publications

2011: Lucilene Arilho Ribeiro; Claudia Danielli Pereira Bertolacini; Rodrigo Gonçalves Quiezi; Antonio Richieri-Costa
A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis.
Clinical dysmorphology 2011;20(3):160-2.
2010: Lucilene Arilho Ribeiro; Rodrigo Gonçalves Quiezi; Adriana Nascimento; Claudia Pereira Bertolacini; Antonio Richieri-Costa
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patients.
American journal of medical genetics. Part A 2010;152A(7):1688-94.
2010: Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in Brazil.
American journal of medical genetics. Part C, Seminars in medical genetics 2010;154C(1):149-57.
2009: Roseli Maria Zechi-Ceide; Lucilene Arilho Ribeiro; Salmo Raskin; Claudia Danielli Pereira Bertolacini; Maria Leine Guion-Almeida; Antonio Richieri-Costa
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes.
American journal of medical genetics. Part A 2009;149A(6):1277-9.
2008: Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Variable phenotypic manifestations of a K44N mutation in the TGIF gene.
Brain & development 2008;30(3):203-5.
2007: Simone Aparecida Capellini; Niura Aparecida de Moura Ribeiro Padula; Lara Cristina Antunes Dos Santos; Maria Dalva Lourenceti; Erika Hasse Carrenho; Lucilene Arilho Ribeiro
[Phonological awareness, working memory, reading and writing performances in familial dyslexia].
Pró-fono : revista de atualização científica 2007;19(4):374-80.
2006: Fedik Rahimov; Lucilene Arilho Ribeiro; Eziquiel de Miranda; Antonio Richieri-Costa; Jeffrey C Murray
GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?
American journal of medical genetics. Part A 2006;140(23):2571-6.
2006: Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype.
American journal of medical genetics. Part A 2006;140(23):2594-7.
2006: Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Holoprosencephaly-like phenotype: clinical and genetic perspectives.
American journal of medical genetics. Part A 2006;140(23):2587-93.
2006: Lucilene Arilho Ribeiro; Jeffrey C Murray; Antonio Richieri-Costa
PTCH mutations in four Brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI.
American journal of medical genetics. Part A 2006;140(23):2584-6.
2006: Lucilene Arilho Ribeiro; Kenia B El-Jaick; Maximilian Muenke; Antonio Richieri-Costa
SIX3 mutations with holoprosencephaly.
American journal of medical genetics. Part A 2006;140(23):2577-83.
2006: Giselda Santiago; Dagma Venturini Marques Abramides; Luciana Paula Maximino De-Vitto; Lucilene Arilho Ribeiro; Silvio Garcia Meira; Antonio Richieri-Costa
Language skills and neuropsychological performance in patients with SHH mutations and a holoprosencephaly-like phenotype.
American journal of medical genetics. Part A 2006;140(19):2085-90.
2006: Melissa Z Antoneli; Sthella Zanchetta; Neivo L Zorzetto; Lucilene Arilho Ribeiro; Antonio Richieri-Costa
Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profiles.
American journal of medical genetics. Part A 2006;140(19):2142-5.
2006: Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2006;43(4):429-34.
2005: Carlos Castro; Patrícia Z Freitas; Melissa Z Antoneli; Giselda Santiago; Lucilene Arilho Ribeiro; Antonio Richieri-Costa
Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia. A new syndrome?
Clinical dysmorphology 2005;14(4):197-201.
2005: Lucilene Arilho Ribeiro; Rita de Cássia M Guerini; Antonio Richieri-Costa
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects.
American journal of medical genetics. Part A 2005;136A(4):350-1.
2005: Lucilene Arilho Ribeiro; Antonio Richieri-Costa
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation.
American journal of medical genetics. Part A 2005;136A(4):346-7.
2005: Antonio Richieri-Costa; Lucilene Arilho Ribeiro
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases.
American journal of medical genetics. Part A 2005;136A(4):352-3.
2005: Lucilene Arilho Ribeiro; Antonio Richieri-Costa
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation.
American journal of medical genetics. Part A 2005;136A(4):348-9.