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1.
J Chem Educ ; 100(9): 3434-3444, 2023 Sep 12.
Artigo em Inglês | MEDLINE | ID: mdl-37720519

RESUMO

The current study describes preliminary findings from the Xavier University of Louisiana Mobile Outreach for Laboratory Enrichment (XULA-MOLE) project, which is a collaboration between Xavier University of Louisiana (XULA), a Historically Black and Catholic University, and participating 9th-12th grade classrooms in the central New Orleans area with a historically underserved student population. The project described here is geared toward providing laboratory enrichment to enhance student learning and impact student career interest in STEM fields, especially in classrooms with a much-needed "hands-on" laboratory experience which is unavailable due to a lack of resources. In this case study, we will present and discuss the inquiry-based laboratory modules for the topic area of acids and bases. These modules were created with careful thought and revision by XULA undergraduate STEM students. The experimental modules were based on the curriculum that participating teachers were discussing in the high-school classroom during the semester. The active-learning efforts were carried out during 6 weeks of the semester to provide a sustained and impactful resource for the participating classrooms. Since both groups of students (XULA-MOLE students and the high school students) were from underrepresented groups there was a strong sense of shared interest and dynamic near-peer mentorship. The project outcomes were measured using both formative and summative assessments indicative of preliminary successes in impacting career interests and increasing the content knowledge of participating high-school students.

2.
Natl Med J India ; 30(2): 73-75, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28816213

RESUMO

BACKGROUND: Presenile cataract is commonly idiopathic in origin. However, patients with presenile cataract could have an underlying genetic abnormality of galactose metabolism. We studied the association, if any, between idiopathic presenile cataract and galactose-1 -phosphate uridyl transferase (GALT) gene mutation. METHODS: We selected 50 patients with idiopathic presenile cataract, <45 years of age, and 50 age- and sex-matched controls for the study. Mutations in the GALT gene were determined by polymerase chain reaction restriction fragment length polymorphism. The classical galactosaemia was characterized by Q188R and K285N mutations, whereas Duarte galactosaemia by N314D mutations (Duarte-2: N314D with IVS5-24G >A and Duarte-1: N314D without IVS5- 24G>A). RESULTS: The most common mutation observed was the N314D (Duarte) mutation. The frequencies of classical and N31 4D alleles in patients with presenile cataract (16%) and controls (26%) were not statistically different (p=0.32, OR 0.54, 95% CI 0.20-1.45). Similarly, there was no statistically significant difference in the frequency distribution of Duarte-1 (p=0.77, OR 0.77, 95% CI 0.23-0.24) and Duarte-2 (p=0.44, OR 0.38, 95% CI 0.07-2.03) galactosaemia mutations in patients and controls. CONCLUSION: Duarte galactosaemia, a milder form of the disease, is more common than classical galactosaemia in the Indian population. Duarte galactosaemia is unlikely to be a causative factor in presenile cataract.


Assuntos
Catarata/genética , Galactosemias/epidemiologia , UTP-Hexose-1-Fosfato Uridililtransferase/genética , Adulto , Fatores Etários , Estudos de Casos e Controles , Catarata/epidemiologia , Catarata/metabolismo , Feminino , Galactose/metabolismo , Galactosemias/genética , Galactosemias/metabolismo , Frequência do Gene , Humanos , Masculino , Polimorfismo de Fragmento de Restrição
3.
Metab Brain Dis ; 30(5): 1291-4, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26037171

RESUMO

Biotinidase deficiency is one of the few treatable inborn errors of metabolism. We describe unique MRI features in two patients with biotinidase deficiency. Brain MRI in case one demonstrated symmetrical diffusion restriction in bilateral hippocampi, parahippocampal gyri, central tegmental tracts, and cerebellar white matter besides other structures that have been reported previously. The second patient was noted to have bilateral symmetrical T2 hyperintensities involving the anterior, lateral and posterior columns of the entire spinal cord on MRI. Knowledge of the varied MRI features of biotinidase deficiency will aid the prompt diagnosis and treatment of a potentially disabling illness, especially in countries where newborn screening is not routinely performed.


Assuntos
Deficiência de Biotinidase/diagnóstico , Deficiência de Biotinidase/metabolismo , Imageamento por Ressonância Magnética , Adolescente , Deficiência de Biotinidase/terapia , Humanos , Lactente , Masculino
4.
Bioorg Med Chem ; 19(24): 7551-8, 2011 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-22055716

RESUMO

The synthesis and structure-activity relationships of 8-substituted-3-[2-(diarylmethoxyethylidenyl)]-8-azabicyclo[3.2.1]octane derivatives were investigated at the dopamine transporter (DAT), the serotonin transporter (SERT) and norepinephrine transporter (NET). The rigid ethylidenyl-8-azabicyclic[3.2.1]octane skeleton imparted modestly stereoselective binding and uptake inhibition at the DAT. Additional structure-activity studies provided a transporter affinity profile that was reminiscent of the structure-activity of GBR 12909. From these studies, the 8-cyclopropylmethyl group has been identified as a unique moiety that imparts high SERT/DAT selectivity. In this study the 8-cyclopropylmethyl derivative 22e (DAT K(i) of 4.0 nM) was among the most potent compounds of the series at the DAT and was the most DAT selective ligand of the series (SERT/DAT: 1060). Similarly, the 8-chlorobenzyl derivative 22g (DAT K(i) of 3.9 nM) was found to be highly selective for the DAT over the NET (NET/DAT: 1358).


Assuntos
Compostos Bicíclicos com Pontes/química , Compostos Bicíclicos com Pontes/farmacologia , Proteínas da Membrana Plasmática de Transporte de Dopamina/metabolismo , Proteínas da Membrana Plasmática de Transporte de Norepinefrina/metabolismo , Octanos/química , Octanos/farmacologia , Proteínas da Membrana Plasmática de Transporte de Serotonina/metabolismo , Animais , Transtornos Relacionados ao Uso de Cocaína/tratamento farmacológico , Humanos , Masculino , Ratos , Ratos Sprague-Dawley , Relação Estrutura-Atividade
5.
Bioorg Med Chem Lett ; 19(24): 6865-8, 2009 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-19896846

RESUMO

A series of 3-arylnortrop-2-enes and 3alpha-arylmethoxy-3beta-arylnortropanes were synthesized and evaluated for binding affinity at monoamine transporters. The 3-(3,4-dichlorophenyl)nortrop-2-ene (6e) exhibited high affinity for the SERT (K(i)=0.3 nM). The 3alpha-arylmethoxy-3beta-arylnortropanes were generally SERT selective with the 3alpha-(3.4-dichlorophenylmethoxy)-3betaphenylnortrop-2-ene (7c) possessing subnanomolar potency (K(i)=0.061 nM). However, 3alpha-(3,4-dichlorophenylmethoxy)-3beta-phenylnortrop-2-ene (7b) exhibited high affinity at all three transporters [(DAT K(i)=22 nM), (SERT K(i)=6 nM) and (NET K(i)=101 nM)].


Assuntos
Proteínas da Membrana Plasmática de Transporte de Dopamina/metabolismo , Proteínas da Membrana Plasmática de Transporte de Norepinefrina/metabolismo , Nortropanos/química , Proteínas da Membrana Plasmática de Transporte de Serotonina/metabolismo , Nortropanos/síntese química , Nortropanos/metabolismo
6.
Acta Crystallogr Sect E Struct Rep Online ; 65(Pt 7): o1667, 2009 Jun 24.
Artigo em Inglês | MEDLINE | ID: mdl-21582927

RESUMO

In the title compound, C(15)H(12)N(2)O(5)S, the benzisothia-zole group is approximately planar (r.m.s. deviation excluding H atoms and the two O atoms bonded to S = 0.023 Å). The dihedral angle between the benzisothia-zole ring and the terminal phenol ring is 84.9 (1)°. In the crystal, mol-ecules are joined by N-H⋯O and O-H⋯O hydrogen bonds, and π-stacking inter-actions are observed between alternating phenol and benzisothia-zole rings [centroid-centroid distances = 3.929 (3) and 3.943 (3) Å].

7.
Interv Neuroradiol ; 24(5): 586-590, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29792091

RESUMO

Carotid rete mirabile is an arterial meshwork, occurring at the cavernous portion of the internal carotid artery (ICA). Rete mirabile in humans is not present during normal development of the intracranial circulation and hence is considered as a collateral pathway that develops as a consequence of segmental agenesis of the ICA. We report three cases of this rare entity encountered at our institute.


Assuntos
Artéria Carótida Interna/anormalidades , Aneurisma Intracraniano/diagnóstico por imagem , Hemorragia Subaracnóidea/diagnóstico por imagem , Hemorragia Subaracnóidea/terapia , Adulto , Angiografia Digital , Artéria Carótida Interna/diagnóstico por imagem , Angiografia Cerebral , Criança , Circulação Colateral , Consanguinidade , Diagnóstico Diferencial , Feminino , Humanos , Angiografia por Ressonância Magnética , Imageamento por Ressonância Magnética
8.
Artigo em Inglês | MEDLINE | ID: mdl-28938856

RESUMO

Hirayama disease is generally considered to be a sporadic disorder, except for a few reports of familial occurrence. In this study, we describe eight patients from four families with cervical flexion induced myelopathy (CFIM)/Hirayama disease (HD) and intra-familial phenotypic variations. All underwent clinical and electrophysiological evaluation, while seven of them had contrast MR imaging of cervical spine in flexion. There was significant intra-familial variability: distal bimelic form in four patients, classical monomelic form in three and proximo-distal form in one. Irrespective of the clinical phenotype, MRI showed characteristic dynamic changes of posterior dural detachment with prominent epidural enhancement extending variably from C3 vertebral level to dorsal spine in six patients. One patient with 28 years of illness, had only lower cervical cord atrophy without dynamic changes while another patient demonstrated forward dural displacement with epidural enhancement even after 38 years of disease duration.


Assuntos
Esclerose Lateral Amiotrófica/patologia , Vértebras Cervicais/patologia , Amplitude de Movimento Articular/fisiologia , Doenças da Medula Espinal/patologia , Adolescente , Adulto , Esclerose Lateral Amiotrófica/diagnóstico , Variação Biológica da População/fisiologia , Humanos , Imageamento por Ressonância Magnética/métodos , Masculino , Pessoa de Meia-Idade , Atrofias Musculares Espinais da Infância/patologia , Adulto Jovem
9.
Oman J Ophthalmol ; 9(2): 110-2, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27433040

RESUMO

A 23-year-old man with a history of alcoholism presented with vomiting, fever, and sharp epigastric pain radiating to the back and flanks. He was diagnosed as a case of acute alcoholic pancreatitis on the basis of clinical findings and investigations. On the next day of presentation, he developed sudden bilateral visual loss. His best-corrected visual acuity was finger counting at one-foot distance in both eyes. He had diffuse whitening in the circumpapillary area, haloes around the retinal vessels (Purtscher flecken) and intra-retinal hemorrhages on ophthalmoscopic examination. Optical coherence tomography revealed bilateral macular edema. These findings were characteristic of Purtscher-like retinopathy. The patient showed systemic and visual improvement at 8 weeks follow-up after receiving the conventional treatment for acute alcoholic pancreatitis. This case emphasizes the importance of fundus examination by an ophthalmologist in the diagnosis of this rare under-diagnosed entity.

10.
Artigo em Inglês | MEDLINE | ID: mdl-27050119

RESUMO

This report aims at describing two new clinical phenotypes associated with classical features of cervical flexion induced myelopathy (CFIM). The description is of a prospective case series of six young males presenting with progressive bilateral proximal/proximo-distal amyotrophy of upper limbs and demonstrating the typical MRI characteristics of Hirayama disease. All underwent detailed clinical, electrophysiologcal and imaging studies. The affected muscles were shoulder girdles and arms in proximal form (n = 2) and the entire upper limbs in proximo-distal form (n = 4). The mean age at onset was 21.0 ± 3.3 years, duration of illness was 6.7 ± 3.4 years, period of progression was 39.0 ± 27.3 months followed by a stable phase of 45.0 ± 50.0 months. All had severe wasting and weakness of affected muscles leading to significant disability. Nerve conduction studies revealed grossly reduced compound muscle action potential amplitudes with neurogenic pattern on electromyography of affected muscles. On MRI all revealed evidence of cervical cord atrophy with signal changes, dural detachment and extensive posterior epidural enhancement (variably from C1 to T2 level). Altered cervical curvature was prominent. In conclusion, hitherto unreported, we describe two additional clinical phenotypes (proximal and proximo-distal forms) of Hirayama disease demonstrating the cardinal imaging features of CFIM.


Assuntos
Vértebras Cervicais/patologia , Doenças da Medula Espinal/etiologia , Atrofias Musculares Espinais da Infância/complicações , Extremidade Superior/fisiopatologia , Adulto , Vértebras Cervicais/diagnóstico por imagem , Eletromiografia , Potencial Evocado Motor/fisiologia , Humanos , Imageamento por Ressonância Magnética , Masculino , Condução Nervosa , Estudos Retrospectivos , Doenças da Medula Espinal/diagnóstico por imagem , Atrofias Musculares Espinais da Infância/diagnóstico por imagem
12.
Middle East Afr J Ophthalmol ; 21(2): 189-92, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24791114

RESUMO

Paradoxical response to anti-tubercular drugs remains a diagnostic dilemma. In India where tuberculosis is quite prevalent, paradoxical response to anti-tubercular treatment (ATT) is either misdiagnosed or under-diagnosed. We report two cases of optochiasmatic arachnoiditis due to paradoxical response in children suffering from tuberculous meningitis. Visual acuity was recorded as no light perception in all eyes of both patients while they were taking 4-drug ATT (isoniazid, rifampicin, pyrazinamide and ethambutol). However their systemic conditions did not worsen. They were treated with intravenous methylprednisolone for five days followed by systemic corticosteroids on a tapering dose for four weeks along with ATT. This case report highlights the importance of early recognition of this sight-threatening complication and timely, effective treatment to prevent permanent blindness.


Assuntos
Antituberculosos/uso terapêutico , Aracnoidite/tratamento farmacológico , Glucocorticoides/uso terapêutico , Metilprednisolona/uso terapêutico , Quiasma Óptico/efeitos dos fármacos , Doenças do Nervo Óptico/tratamento farmacológico , Tuberculose Meníngea/tratamento farmacológico , Aracnoidite/diagnóstico , Criança , Pré-Escolar , Etambutol/uso terapêutico , Humanos , Infusões Intravenosas , Isoniazida/uso terapêutico , Imageamento por Ressonância Magnética , Masculino , Quiasma Óptico/patologia , Doenças do Nervo Óptico/diagnóstico , Pirazinamida/uso terapêutico , Rifampina/uso terapêutico , Resultado do Tratamento , Tuberculose Meníngea/diagnóstico , Acuidade Visual
13.
Indian J Dent Res ; 24(6): 784-6, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24552950

RESUMO

AIM: To determine labial and lingual plate width at extraction site, using extracted tooth. MATERIALS AND METHODS: Pre-extraction ridge mapping and arch impression using putty consistency elastomeric impression material is recorded, followed by atraumatic tooth extraction, extracted tooth is cleaned and reoriented in the earlier recorded elastomeric putty impression. The cast obtained is used to measure bone width. RESULTS: The amount of available labial and palatal bone of an extracted socket can be assessed accurately. CONCLUSION: This technique will help the surgeon understand the thickness of labial plate especially the apical region without reflecting the flap, also aid in selection of proper dimension of dental implant, and if bone graft is needed.


Assuntos
Processo Alveolar/patologia , Carga Imediata em Implante Dentário , Alvéolo Dental/cirurgia , Humanos
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