Found: 34
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Steven Fabian. Making Identity on the Swahili Coast: Urban Life, Community, and Belonging in Bagamoyo.
- Published in:
- 2021
- By:
- Publication type:
- Book Review
Commoners in the process of Islamization: reassessing their role in the light of evidence from southeastern Tanzania.
- Published in:
- Journal of Global History, 2008, v. 3, n. 2, p. 227, doi. 10.1017/S1740022808002623
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- Publication type:
- Article
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 9, p. e129, doi. 10.1111/epi.13076
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- Publication type:
- Article
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy.
- Published in:
- Epilepsia (Series 4), 2013, v. 54, n. 2, p. 265, doi. 10.1111/epi.12084
- By:
- Publication type:
- Article
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
- Published in:
- Epilepsia (Series 4), 2012, v. 53, n. 2, p. 308, doi. 10.1111/j.1528-1167.2011.03379.x
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- Publication type:
- Article
The Nature of German Imperialism: Conservation and the Politics of Wildlife in Colonial East Africa.
- Published in:
- Conservation & Society, 2020, v. 18, n. 2, p. 204, doi. 10.4103/cs.cs_20_48
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- Publication type:
- Article
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes.
- Published in:
- Nature Genetics, 2014, v. 46, n. 12, p. 1327, doi. 10.1038/ng.3130
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- Publication type:
- Article
INTRODUCTION: PERFORMING CITIZENSHIP AND ENACTING EXCLUSION ON AFRICA'S INDIAN OCEAN LITTORAL.
- Published in:
- Journal of African History, 2014, v. 55, n. 2, p. 161, doi. 10.1017/S0021853714000139
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- Publication type:
- Article
AN ANTHROPOLOGIST OF AFRICA IN BRITAIN AND IN NAZI GERMANY.
- Published in:
- 2005
- By:
- Publication type:
- Book Review
TRADERS, 'BIG MEN' AND PROPHETS: POLITICAL CONTINUITY AND CRISIS IN THE MAJI MAJI REBELLION IN SOUTHEAST TANZANIA.
- Published in:
- Journal of African History, 2004, v. 45, n. 1, p. 1, doi. 10.1017/S0021853703008545
- By:
- Publication type:
- Article
Religious Anxieties in Two Marginal Regions.
- Published in:
- Comparative Studies of South Asia, Africa, & the Middle East, 2013, v. 33, n. 1, p. 102, doi. 10.1215/1089201X-2072748
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- Publication type:
- Article
Female Seclusion in the Aftermath of Slavery on the Southern Swahili Coast: Transformations of Slavery in Unexpected Places.
- Published in:
- International Journal of African Historical Studies, 2015, v. 48, n. 2, p. 209
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- Publication type:
- Article
Remembering Nyerere: Political rhetoric and dissent in contemporary Tanzania.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Season of Rains: Africa in the world.
- Published in:
- 2012
- By:
- Publication type:
- Book Review
Africa's development in historical perspective.
- Published in:
- 2016
- By:
- Publication type:
- Book Review
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy.
- Published in:
- Epilepsia Open, 2019, v. 4, n. 3, p. 420, doi. 10.1002/epi4.12349
- By:
- Publication type:
- Article
Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.
- Published in:
- Epilepsia Open, 2017, v. 2, n. 3, p. 334, doi. 10.1002/epi4.12068
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- Publication type:
- Article
Tanzania's Authoritarian Turn: Less Sudden Than It Seems.
- Published in:
- Current History, 2021, v. 120, n. 826, p. 189
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- Publication type:
- Article
Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study.
- Published in:
- Epilepsia (Series 4), 2022, v. 63, n. 3, p. 723, doi. 10.1111/epi.17166
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- Publication type:
- Article
Testing association of rare genetic variants with resistance to three common antiseizure medications.
- Published in:
- Epilepsia (Series 4), 2020, v. 61, n. 4, p. 657, doi. 10.1111/epi.16467
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- Publication type:
- Article
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
- Published in:
- Epilepsia (Series 4), 2019, v. 60, n. 5, p. e31, doi. 10.1111/epi.14657
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- Publication type:
- Article
Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis.
- Published in:
- Epilepsia (Series 4), 2017, v. 58, n. 10, p. 1734, doi. 10.1111/epi.13871
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- Publication type:
- Article
Reply.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
- Published in:
- 2016
- By:
- Publication type:
- journal article
DEPDC5 mutations in genetic focal epilepsies of childhood.
- Published in:
- Annals of Neurology, 2014, v. 75, n. 5, p. 788, doi. 10.1002/ana.24127
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- Publication type:
- Article
Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature.
- Published in:
- Journal of Neurology, 2014, v. 261, n. 10, p. 1881, doi. 10.1007/s00415-014-7433-5
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- Publication type:
- Article
PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
- Published in:
- Journal of Neurology, 2013, v. 260, n. 5, p. 1234, doi. 10.1007/s00415-012-6777-y
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- Publication type:
- Article
Galanin pathogenic mutations in temporal lobe epilepsy.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 11, p. 3082, doi. 10.1093/hmg/ddv060
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- Publication type:
- Article
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes.
- Published in:
- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0150426
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- Publication type:
- Article
In Pursuit of Freedom: Oaths, Slave Agency, and the Abolition of Slavery in Western Tanzania, 1905–1930.
- Published in:
- Law & History Review, 2024, v. 42, n. 1, p. 119, doi. 10.1017/S0738248023000615
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- Publication type:
- Article
PRRT2 Mutations are the major cause of benign familial infantile seizures.
- Published in:
- Human Mutation, 2012, v. 33, n. 10, p. 1439, doi. 10.1002/humu.22126
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- Publication type:
- Article