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Deformities in reared cobia, Rachycentron canadum L. and grouper, Epinephelus marginatus, in São Paulo state coast, Brazil: case report Arq. Bras. Med. Vet. Zootec.
Engrácia Filho,J.R.; Shimada,M.T.; Yunis-Aguinaga,J.; Ramos-Espinoza,F.C.; Moraes,F.R.; Moraes,J.R.E..
ABSTRACT Skeletal deformities are frequent problems in cultured fish populations due mainly to unfavorable abiotic conditions, inappropriate nutrition, and genetic factors. These may cause erratic swimming, decrease of conversion rate, growth, and market value. The aim of this case report was to present the occurrence of deformities in juvenile cobia and groupers from an offshore marine farm in Ilhabela, São Paulo, Brazil. Nine cobias and seven juvenile groupers, that presented deformities, were euthanized and fixed in 10% formaldehyde. They were tagged, processed, and stained with "Alcian Blue" (AB) and "Alizarin Red-S" (ARS) for visualization of cartilage and bone tissue, respectively. After evisceration, radiographic examination was performed. The...
Tipo: Info:eu-repo/semantics/report Palavras-chave: Operculum atrophy; Kyphosis; Scoliosis; Saddleback syndrome.
Ano: 2018 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0102-09352018000501565
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First record of partial albinism and scoliosis in Odontophrynus occidentalis tadpoles (Anura: Cycloramphidae) BABT
Sanabria,Eduardo Alfredo; Quiroga,Lorena Beatriz; Laspiur,Alejandro.
Albinism has been widely reported for diverse group of vertebrates. However, scoliosis is a rare abnormality. In this work, the first record of partial albinism and scoliosis case in tadpole of the frog Odontophrynus occidentalis is being presented. The individual was captured in Quebrada de las Flores, Sierra Pie de Palo, Caucete Department, San Juan Province, Argentina.
Tipo: Info:eu-repo/semantics/article Palavras-chave: Albinism; Scoliosis; Odontophrynus occidentalis; San Juan; Argentina.
Ano: 2010 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132010000300019
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High frequencies of plexiform neurofibromas, mental retardation, learning difficulties, and scoliosis in Brazilian patients with neurofibromatosis type 1 BJMBR
Trovó-Marqui,A.B.; Goloni-Bertollo,E.M.; Valério,N.I.; Pavarino-Bertelli,E.C.; Muniz,M.P.; Teixeira,M.F.; Antonio,J.R.; Tajara,E.H..
A clinical study of Brazilian patients with neurofibromatosis type 1 (NF1) was performed in a multidisciplinary Neurofibromatosis Program called CEPAN (Center of Research and Service in Neurofibromatosis). Among 55 patients (60% females, 40% males) who met the NIH criteria for the diagnosis of NF1, 98% had more than six café-au-lait patches, 94.5% had axillary freckling, 45% had inguinal freckling, and 87.5% had Lisch nodules. Cutaneous neurofibromas were observed in 96%, and 40% presented plexiform neurofibromas. A positive family history of NF1 was found in 60%, and mental retardation occurred in 35%. Some degree of scoliosis was noted in 49%, 51% had macrocephaly, 40% had short stature, 76% had learning difficulties, and 2% had optic gliomas....
Tipo: Info:eu-repo/semantics/article Palavras-chave: Neurofibromatosis type I; Plexiform neurofibroma; Mental retardation; Learning difficulties; Scoliosis.
Ano: 2005 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000900020
Registros recuperados: 3
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