Fahmida Essop

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 9

Top Topics

Peritoneal Dialysis

African American

Ejection Fraction

Top Venues

European journal of human genetics : EJHG

Tremor and other hyperkinetic movements (New York, N.Y.)

Familial cancer

This page only lists publications with an associated author ORCID identifier.

Publications

Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Abdoulaye Bocoum, Madani Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha, Cheick A K Cissé, Alassane Baneye Maiga, Amanda Krause, Guida Landouré, null null
The First Case of Huntington's Disease like 2 in Mali, West Africa. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Abdoulaye Bocoum, Madani Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha, Cheick A K Cissé, Alassane Baneye Maiga, Amanda Krause, Guida Landouré, null null
The First Case of Huntington's Disease like 2 in Mali, West Africa. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Abdoulaye Bocoum, Madani Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha, Cheick A K Cissé, Alassane Baneye Maiga, Amanda Krause, Guida Landouré, null null
The First Case of Huntington's Disease like 2 in Mali, West Africa. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Shelley Macaulay, Quintin Clive Goodyear, Mia Kruger, Wenlong Carl Chen, Fahmida Essop, Amanda Krause
The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome. Familial cancer 17 (4) (2019)