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  • 1
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1990
    In:  Arquivos de Neuro-Psiquiatria Vol. 48, No. 4 ( 1990-12), p. 502-504
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 48, No. 4 ( 1990-12), p. 502-504
    Abstract: Movement disorders, mostly dystonia, sometimes occur in heterozygotes for Wilson's disease (WD). A patient with metabolic abnormalities suggestive of heterozigose for WD and dystonia is reported. His niece showed the typical neurological and metabolic abnormalities of WD. This rare coincidence and the etiopathogenic mechanisms involved are discussed .
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1990
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  • 2
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1975
    In:  Arquivos de Neuro-Psiquiatria Vol. 33, No. 2 ( 1975-06), p. 105-118
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 33, No. 2 ( 1975-06), p. 105-118
    Abstract: Os autores apresentam uma revisão de 21 pacientes com diagnóstico de neuropatia amilóide tipo I, firmado sobre os dados epidemiológicos, a evolução clínica e os achados histopatológicos. Chamam a atenção para a possibilidade de comprometimento de vários nervos cranianos, para a gravidade do quadro digestivo, a precocidade dos distúrbios neurovegetativos e a incidência relativamente alta de sintomatologia cardíaca. Constituem contribuição para o melhor conhecimento da afecção, os estudos sobre a síndrome digestiva feitos através de exames radiológicos e dos testes de absorção de vitamina B12 e trioleína radioativas.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1975
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  • 3
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1956
    In:  Arquivos de Neuro-Psiquiatria Vol. 14, No. 4 ( 1956-12), p. 285-298
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 14, No. 4 ( 1956-12), p. 285-298
    Abstract: With the purpose of establishing the normal figure of the distance between the odontoid tip and the Fischgold-Metzger's bimastoid line - a useful reference for the radiological diagnosis of basilar impression - the authors make the statistical study of the measurements on 127 craniograms of patients without occipito-cervical malformations and on 11 cases of basilar impression diagnosed clinical and radiologically. The correlations of that distance with age and with the distance from the odontoid tip to the McGregor's basal line are studied. The authors conclude that: 1) Above 10 years of age, the average distance from the odontoid tip to the bimastoid line is normally +0.56 ± 5.79 mm., the fiducial limits being -10.79 and +11.91 mm. Therefore, figures above 12 mm. must be considered as radiological index of basilar impression. 2) Correlation was observed between the distances from the odontoid tip to McGregor's and Fischgold-Metzger's lines, in 120 normal cases, above 10 years of age. 3) There was no difference between sexes in relation to the distance from the odontoid tip to the bimastoid line. 4) At least until 20 years of age there is correlation between this distance and age. Therefore, under that age, the diagnosis of basilar impression must be made in presence of lesser figures of this distance, the upper normal limit being around +8 mm. 5) In cases of basilar impression, the average distance from the odontoid tip to the bimastoid line was +21.09 ± 10.03 mm., significantly greater than the average of cases without occipito-cervical anomalies. 6) There was no correlation between the degree of basilar impression and the age and between the distances from the odontoid tip and McGregor's and Fischgold-Metzger's lines in the cases of basilar impression.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1956
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  • 4
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1951
    In:  Arquivos de Neuro-Psiquiatria Vol. 9, No. 3 ( 1951-09), p. 203-222
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 9, No. 3 ( 1951-09), p. 203-222
    Abstract: The authors emphasize the dangers of diagnostic errors in the cases of neuroblastomycosis, whether in the meningoencephalic or the tumoral forms. Paracoccidioidosis and cryptococcosis are studied. After a clinical characterization of paracoccidioidosis, the authors stress the scarceness of its nervous forms (1,2 per cent of 84 necropsies of this mycosis performed at the Department of Pathology of the Faculty of Medicine of São Paulo). In the literature there are but 12 cases reported. Casiello and Class' is the only case where the diagnosis was made during life; the other cases were necroscopic findings or unexpected histopathologic data after the patients had been operated on por presumptive tumors. The authors report 2 cases of paracoccidioidosis of the nervous system. In the first one, showing meningo-myelo-radiculitis, the parasite was identified in the sputum; the second patient exhibited a syndrome of spinal compression, whose pathogeny is discussed by the authors (lymphatic infiltration of the epidural cervical space? lymphatic infiltration of the spinal cord? allergic diffuse serous inflammation of the spinal cord caused by the ganglionar focus?) ; the paracoccidioidal etiology was attested by bactériologie examination and biopsy of cervical lymph nodes. After clinical comments on cryptococcosis, the authors report a case of subacute meningoencephalomyelitis, which was diagnosed as paracoccidioidal by the mycologie examination of the cerebrospinal fluid; this patient, although treated with high doses of sulfonamides and thiosemicarbarsone, died after two remissions of the symptomatology; the necroscopic examination disclosed the real nature of the neurological changes, which were diagnosed as torular granuloma. In all cases the neurosurgical aspect of the symptomatology was impressive. Neverthless, the diagnosis of paracoccidioidosis imposed the treatment with sulfadiazine, sulfamerazine, specific vaccine and thiosemicarbarsone. Results were remarkable in case 2, where treatment was earlier started; case 1 also showed improvement. In case 3, transient improvement followed the treatment, but, after two years of disease, the patient died. The authors conclude that nervous blastomycosis must be taken on account in neurosurgical considerations. In paracoccidioidosis massive doses of sulfa drugs associated to specific vaccine, however, will be the first therapeutic approach. In the treatment of cryptococcosis streptothricin and actidione are worth trying according to experimental studies. Surgery is indicated only in the cases where the site or developmental conditions of the disease demand urgent resolution.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1951
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  • 5
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 50, No. 1 ( 1992-03), p. 99-103
    Abstract: Three patients with symptoms and signs of hepatolenticular degeneration (HLD) who developed serious renal side effects of D-penicillamine (DP) had their therapeutic schedule changed to zinc. Patient 1, a 55 year-old man had been well until 12 years old, when skeletal changes (osteomalacia) due to tubular renal disturbance began. His diagnosis of HLD had first been established at age of 32 when he presented with «wing-beat» tremor. He was then begun on DP and his neurological symptons resolved within one year of initiating therapy but skeletal abnormalities remained unchanged as a sequel. During the next 22 years the patient was continued on DP therapy but with poor compliance. Then the reapperance of his neurological manifestations occurred several times. By the age of 53, after one year without therapy, his neurological status has worse. DP was reinstituted but some weeks later his renal laboratorial parameters became serevely affected. DP was discontinued and zinc sulfate (220mg three times daily) was introduced. On this therapeutic regimen his renal laboratorial parameters returned to previous level after one month. Within one year on this therapeutic regimen neurological manifestations were resolved. After 31 months on zinc treatment he remains neurologically asymptomatic and his renal function is satisfactory. Patient 2, a 41 years old woman had been her diagnosis of HLD at age of 20, when following the diagnosis of the disease in her old brother, she was found to have the laboratorial features of HLD and bilateral Kayser-Fleischer rings. DP treatment was recommended at that time but she quitted the follow-up. When she. was 23, an esophageal variceal bleeding occurred. At the age of 30 she started DP treatment. During 9 years the patient, under regular use of the drug remained assymptomatic. At the age of 39 she developed acute renal failure due to penicillamine-induced immune complex nephropathy. DP was then stopped and prednisone introduced. After 4 months, as renal function returned to normal, prednisone was discontinued and zinc sulphate (220mg three times daily) introduced. She remained asymptomatic for 38 months. By the age of 41 a relapse of renal manifestations occurred, and she died months later. Patient 3, a 20 year-old man developed hemolytic anemia as the single manifestation of HLD at 16. DP was introduced with excellent results. Neverthless, 4 months later, with the appearance of severe renal side--effects, this drug was replaced by zinc sulphate (220mg three times daily). After 11 months under this therapeutic schedule he was hematologically asymptomatic but an epigastric distress appeared. Zinc sulphate was discontinued and zinc acetate (170mg three times daily) was introduced. Since that time, after 30 months of treatment with zinc, he remains asymptomatic and Kayser-Fleisher rings disappeared. A review of zinc salts therapy of HLD is presented and discussed.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1992
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  • 6
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1953
    In:  Arquivos de Neuro-Psiquiatria Vol. 11, No. 4 ( 1953-12), p. 371-380
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 11, No. 4 ( 1953-12), p. 371-380
    Abstract: In order to know the influence of intravenous injection of 50 per cent glucose solutions on the sugar contents of the cerebrospinal fluid, after estimating the error of the laboratory method the authors studied in detail such effects in three groups of patients: group 1, for controlling the results (3 cases) ; group 2, including 5 patients with normal and 5 with abnormal (presenting meningitic and/or parenchymatous changes) fluids; group 3, including 10 patients with normal and 10 with abnormal fluids. In group 1 no glucose was injected; in group 2, 10 gm were administered; in group 3, 50 gm were injected. The method of study consisted essentially of: a) simultaneous withdrawal of blood and fluid, in fasting conditions, for determination of the initial levels; b) intravenous injection of 50 percent glucose solution; c) 15, 30, 45, 60, 120, 180 and 240 minutes later, other samples of blood and fluid were withdrawn from each patient. The results were submitted to statistical analysis. The oscilations of the average levels obtained in groups 1 and 2 were comparable to those due to the experimental error. The differences between the initial mean and the average contents 15 and 30 minutes after the injection of 10 gm glucose were not statistically significant; in the patients receiving 50 gm, only after 30 minutes the average content differed significantly from the initial mean. The linear regression equations relating time to the blood and cerebrospinal fluid sugar contents were calculated. The ratios between fluid and blood sugar contents were analysed. In 10 cases of group 3 the blood and fluid sugar contents before and 24 hours after the glucose injection were compared. The authors draw the following conclusions: 1. The intravenous injection of 10 gm glucose does not influence significantly the cerebrospinal fluid sugar content. 2. After the intravenous injection of 50 gm glucose it is observed, during the first hour, a uniform increase of the fluid sugar contents, mostly in the patients with abnormal fluid, probably owing to greater permeability of the blood-brain barrier. 3. The ratios between cerebrospinal fluid and blood sugar contents (CSF/B) showed progressive increase in the patients with abnormal fluid 15 to 120 minutes after the injection of 10 gm glucose. 4. The CSF/B ratios showed progressive increase both in the patients with normal and abnormal fluid, 15 to 120 minutes after the injection of 50 gm glucose; the difference between the regression coefficientes of these two groups was not significant. 5. The average initial ratio between the cerebrospinal fluid and the blood sugar contents, in 29 patients, was 0.617 ± 0.129. 6. The increase of the cerebrospinal fluid sugar content after the intravenous injection of 50 gm glucose lasted 4 hours at least. 7. There was no significant difference between the blood and cerebrospinal fluid sugar contents before and 24 hours after the intravenous injection of 50 gm glucose.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1953
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  • 7
    Online Resource
    Online Resource
    Hindawi Limited ; 1983
    In:  Acta Neurologica Scandinavica Vol. 67, No. 5 ( 1983-05), p. 305-311
    In: Acta Neurologica Scandinavica, Hindawi Limited, Vol. 67, No. 5 ( 1983-05), p. 305-311
    Type of Medium: Online Resource
    ISSN: 0001-6314 , 1600-0404
    URL: Issue
    RVK:
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 1983
    detail.hit.zdb_id: 2001898-8
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  • 8
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 25, No. 4 ( 1967-12), p. 255-268
    Abstract: São apresentados 31 casos de leucoencefalite esclerosante subaguda, cujo diagnóstico se baseou no quadro clínico, no acentuado aumento das globulinas y no líquido cefalorraqueano, nas características alterações do eletrencefalograma e no estudo anátomo-patológico. Foram encontrados corpúsculos de inclusão intracelular mediante o estudo necroscópico de 8 entre 13 casos e o exame histopatológico de 1 entre 7 biopsias cerebrais. A média etária foi de 11,7 anos, com os limites de 3 a 22 anos. O sexo masculino predominou nitidamente sobre o feminino (23:8). Os pacientes provenientes da zona rural constituíram a maioria dos casos (77,4%). A análise da distribuição geográfica não demonstrou predomínio regional definido. Não foi observada influência estacional sôbre o início da moléstia. Em 16 casos acompanhados até o óbito, a duração média foi de 7 meses, com uma faixa de 2 a 20 meses. No quadro clínico sobressaiu a presença eonstante de mioclonias ou perdas de tono, e de alterações psíquicas. O primeiro sintoma foi representado por distúrbios psíquicos em 55,6% dos pacientes, por mioclonias em 35,5%o e por convulsões do tipo grande mal em 33,3%. Rigidez e sinais piramidais foram muito freqüentes, sendo rara a síndrome cerebelar. Alterações oftalmoscópicas (edema ou palidez de papila, coroidite) foram verificadas em um terço dos casos. Em 2 casos o início da moléstia coincidiu com uma epizootia de galinhas. Os valores do cobre sangüíneo, determinados em 8 casos, situaram-se sempre acima da faixa normal, enquanto a ceruloplasmina permaneceu dentro dos limites normais. Os valores do enxofre sangüíneo revelaram-se elevados em 3 pacientes examinados. Os níveis da magnesemia mostraram-se variáveis em 6 pacientes estudados.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1967
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  • 9
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1963
    In:  Arquivos de Neuro-Psiquiatria Vol. 21, No. 2 ( 1963-06), p. 87-95
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 21, No. 2 ( 1963-06), p. 87-95
    Abstract: The present study was carried out in order to investigate the nature of the increase in the cerebrospinal fluid (CSF) protein content described in diabetic neuropathy. The CSF proteins were studied in 22 patients with clinical signs of diabetic neuropathy. The total protein content and the electrophoretic pattern (paper electrophoresis) of the proteins were studied in one CSF sample of each patient. The CSF sample was collected through lumbar puncture. For comparative purposes, the total protein content and the electrophoretic pattern of the blood serum proteins were determined in 17 patients. For the same purpose the impairment of the nervous system was evaluated in a semi-quantitative way. The CSF protein concentration was increased in 7 cases (32%). The increases were slight. The electrophoretic patterns were found to be similar to those found in normal conditions. The relative values found for each of the protein fractions were increased in some instances. Such increases were slight and did not change the protein pattern of the CSF. Among these changes, that regarding the y-globulin was observed in 3 cases. The CSF protein pattern did not show changes related to the total protein content of the sample. Changes in the serum protein pattern did not induce changes in the CSF protein pattern. The correlation between the total protein content of CSF and serum was not statistically significant. In the cases studied no statistically significant correlation between the degree of neurological involvement and the CSF proteins was found. However, the data suggest a trend to correlation between the neurological picture and the total protein content of the CSF, particularly with β-globulin.The results show that the increase in the total protein content of the CSF in diabetic neuropathy is not related to changes regarding one or more of the protein fractions of CSF. It is not dependent also on the protein concentration in the blood serum and/or the changes found in its protein pattern. The degree of the nervous impairment in itself cannot be directly related to the increase in the CSF proteins. The importance of damage in the blood-CSF barrier is pointed out by data of the literature concerning the protein fractions in diabetic patients. Such damage cannot be excluded in the discussion of the results found. Its presence would enhance the passage of proteins to the CSF, thus resulting an increase in the total protein content. Changes in the protein pattern in such conditions are absent or slight, as it was found in the cases studied.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1963
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  • 10
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 1963
    In:  Arquivos de Neuro-Psiquiatria Vol. 21, No. 2 ( 1963-06), p. 77-86
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 21, No. 2 ( 1963-06), p. 77-86
    Abstract: As formas medulares da neurocisticercose são relativamente raras (2,7% de 296 casos desta parasitose registrados na Clínica Neurológica da Faculdade de Medicina da USP). Em revisão da literatura só encontramos 42 casos, na maioria dêles ocorrendo associação com sintomas encefálicos. São discutidas as razões desta baixa incidência, assim como as possíveis vias seguidas pelo parasito a fim de alcançar a medula. Após reverem os primeiros casos registrados na literatura, os autores destacam as principais síndromes (meningomielítica, tabetiforme e de compressão medular) e alguns dos caracteres clínicos e anátomo-patológicos da cisticercose medular. São relatados 9 casos de cisticercose medular. O diagnóstico baseou-se em dados laboratoriais (especialmente a positividade da reação de fixação de complemento para cisticercose no líquido cefalorraqueano) ou nos resultados cirúrgicos. Outros aspectos do exame do líquido cefalorraqueano (presença de eosinófilos, proteinorraquia e resultados das provas manométricas) são comentados. A perimielografia demonstrou existência de bloqueio do canal raqueano em 5 casos. Três dêstes pacientes foram submetidos a la-minectomia, com resultados variáveis. O quadro neurológico predominante foi o de compressão da medula e/ou das raízes nervosas (4 casos). Dois pacientes apresentavam uma síndrome cordonal posterior que simulava a tabes dorsal. Dois outros pacientes apresentavam um quadro de meningomielite não sistematizada. Um paciente tinha uma síndrome sugestiva de mielose funicular, mas a presença de sintomas cerebrais e os resultados dos exames de laboratório levaram a considerar a cisticercose como a etiologia mais provável.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 1963
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