Diabetic polyneuropathy with/out neuropathic pain in Mali: A cross-sectional study in two reference diabetes treatment centers in Bamako (Mali), Western Africa von Maiga, Youssoufa, Diallo, Salimata, Konipo, Fatoumata Dite Nènè, Sangho, Oumar, Sangaré, Modibo, Diallo, Seybou H, Mahamadou, Saliou, Péréon, Yann, Giumelli, Bernard, Coulibaly, Awa, Daou, Mariam, Traoré, Zoumana, Sow Sylla, Djeneba, Albakaye, Mohamed, Guinto, Cheick Oumar, Ouologem, Madani, Sissoko, Adama S, Traoré, Hamar A, Coulibaly, Souleymane Papa, Damier, Philippe, Attal, Nadine, Nizard, Julien

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Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings von Cissé, Lassana, Bamba, Salia, Diallo, Seybou H, Ji, Weizhen, Dembélé, Mohamed Emile, Yalcouyé, Abdoulaye, Coulibaly, Toumany, Traoré, Ibrahima, Jeffries, Lauren, Diarra, Salimata, Maiga, Alassane Dit Baneye, Diallo, Salimata, Nimaga, Karamoko, Touré, Amadou, Traoré, Oumou, Kotioumbé, Mahamadou, Mis, Emily Kathryn, Cissé, Cheick Abdel Kader, Guinto, Cheick Oumar, Fischbeck, Kenneth H, Khokha, Mustafa K, Lakhani, Saquib A, Landouré, Guida

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A rare case of thyrotoxic periodic paralysis revealing Graves' disease in a young Malian von Dembélé, Mohamed Emile, Yalcouyé, Abdoulaye, Cissoko, Mamadou, Cissé, Lassana, Guinto, Cheick Oumar, Landouré, Guida

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A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl von Cissé, Lassana, Yalcouyé, Abdoulaye, Touré, Kadidia Oumar, Coulibaly, Youlouza, Maiga, Alassane Baneye, Bamba, Salia, Diallo, Dramane, Diarra, Salimata, Taméga, Abdoulaye, Traoré, Oumou, Kotioumbé, Mahamadou, Sangaré, Moussa Aly, Ba, Hamidou Oumar, Simaga, Assiatou, Koné, Fatogoma Issa, Samassekou, Oumar, Koné, Amadou, Guinto, Cheick Oumar, Landouré, Guida

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Cauda Equina Syndrome and Profound Hearing Loss After Spinal Anesthesia with Isobaric Bupivacaine von Moussa, Traore, Abdoulaye, Diallo, Youssouf, Coulibaly, Oumar, Guinto Cheick, Karim, Timbo Samba, Traore, Thomas Jeannette

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A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family von Maiga, Alassane Baneye, Pamanta, Ibrahim, Bamba, Salia, Cissé, Lassana, Diarra, Salimata, Touré, Sidi, Yalcouyé, Abdoulaye, Diallo, Seydou, Diallo, Salimata, Kané, Fousseyni, Diallo, Seybou Hassane, Ba, Hamidou Oumar, Guinto, Cheick Oumar, Fischbeck, Kenneth, Landoure, Guida, Cissé, Idrissa Ahmadou

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Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali von Yalcouyé, Abdoulaye, Traoré, Oumou, Taméga, Abdoulaye, Maïga, Alassane B, Kané, Fousseyni, Oluwole, Oluwafemi G, Guinto, Cheick Oumar, Kéita, Mohamed, Timbo, Samba Karim, DeKock, Carmen, Landouré, Guida, Wonkam, Ambroise

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Validation of two parent-reported autism spectrum disorders screening tools M-CHAT-R and SCQ in Bamako, Mali von Sangare, Modibo, Toure, Hamza B., Toure, Amadou, Karembe, Adama, Dolo, Housseini, Coulibaly, Yaya I., Kouyate, Modibo, Traore, Kadiatou, Diakité, Seidina A., Coulibaly, Souleymane, Togora, Arouna, Guinto, Cheick Oumar, Awandare, Gordon A., Doumbia, Seydou, Diakite, Mahamadou, Geschwind, Daniel H.

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Neuropathic pain in Mali: The current situation, comprehensive hypothesis, which therapeutic strategy for Africa? von Maiga, Youssoufa, Sangho, Oumar, Konipo, Fatoumata, Diallo, Seybou, Coulibaly, Souleymane Dit Papa, Sangare, Modibo, Péréon, Yann, Giumelli, Bernard, Sanou, Martin, Coulibaly, Awa, Diallo, Salimata, Daou, Mariam, Traoré, Zoumana, Albakaye, Mohamed, Traoré, Hamar A., Guinto, Cheick Oumar, Ouologem, Madani, Kuate-Tegueu, Callixte, Bouhassira, Didier, Cowan, Robert, Nizard, Julien

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Epidemiological and clinical aspects of HIV associated dementia at the University Hospital of Point G von Guinto, Cheick Oumar, Coulibaly, Toumany, Berthé, S, Karembe, Mamadou, Traoré, S, Coulibaly, Thomas, Sissoko, Adama, Landoure, Guida, Dao, Sounkalo, Traoré, Moussa

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Non-motor signs in patients with Parkinson's disease at the University Hospital of Point “G”, Mali von Maïga, Boubacar, Koné, Aïssata, Landouré, Guida, Coulibaly, Toumany, Sangaré, Modibo, Dembélé, Kekouta, Diop, Marième Soda, Cissé, Lassana, Dadah, Sami Mohamed Lemine, Konaté, Mamadou, Coulibaly, Catherine, Sissoko, Adama Seydou, Coulibaly, Thomas, Karambé, Mamadou, Guinto, Cheick Oumar, Moustapha Ndiaye, M., Ndiaye, Mouhamadou Mansour, Traoré, Moussa

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Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study von Rizig, Mie, Bandres-Ciga, Sara, Levine, Kristin S, Adeniji, Olaleye Akinmola, Agabi, Osigwe Paul, Arigbodi, Ohwotemu Michael, Erameh, Cyril Oshomah, Okunoye, Olaitan, Komolafe, Morenikeji Adeyoyin, Odeniyi, Olanike Adedoyin, Ojini, Francis Ibe, D'Souza, Andrea M, Osemwegie, Nosakhare, Leonard, Hampton L, Ozomma, Simon Izuchukwu, Zubair, Yusuf Agboola, Abiodun, Oladunni, Akinyemi, Rufus, Ali, Mohammed, Bello, Abiodun, Erameh, Cyril, Farombi, Temitope, Imarhiagbe, Frank, Iwuozo, Emmanuel, Nwazor, Ernest, Ojini, Francis, Onwuegbuzie, Gerald, Ozomma, Simon, Zubair, Yusuf, Gueumekane Bila lamou, Eric, Shalash, Ali, Khedr, Eman, El-Jaafary, Shaimaa, Hamed, Sharifa, Melka Oda, Dereje, Debebe Gelan, Yohanesse, Charway-Felli, Augustina, Stephen Sarfo, Fred, Koita, Abdou, Bell, Abiodun, Adebowale, Akintunde A., Akpekpe, John, Agu, Christian, Agabi Osigwe, Paul, Balarabe, Salisu, Williams, Uduak, Hilaire Dominique, Ewodo Touna, Mochan, Andre, Ben Djebara, Mouna, Kacem, Imen, Mkada, Imen, Atadzhanov, Masharip, Jama, Fatumah, Hall, Deborah A., Warren, Natalie, Chauppeta, Brian, Rawls, Ashley, O'Grady, Alyssa, Sherer, Todd, Blauwendraat, Cornelis, Brice, Alexis, Illarionova, Anastasia, Quattrone, Andrea, Kishore, Asha, Ahmad-Annuar, Azlina, Mollenhauer, Brit, Carroll, Camille, Rieder, Carlos, KP, Divya, Fon, Edward A., Gatto, Emilia M, Xiromerisiou, Georgia, Hiu-Fai Chan, Germaine, Kaishibayeva, Gulnaz, Leonard, Hampton, Iwaki, Hirotaka, Chen, Honglei, F. Mata, Ignacio, Aasly, Jan O., Kim, Jonggeol Jeff, Lohmann, Katja, Kumar, Kishore, Shulman, Lisa, Parnetti, Lucilla, Periñan Tocino, Maria Teresa, Ibrahim Norlinah, Mohamed, Williams, Nigel, Kaiyrzhanov, Rauan, Krüger, Rejko, Wu, Ruey-Meei, Bandres-Ciga, Sara, Wu, Serena, Lim, Shen-Yang, Ertan, Sibel, Foroud, Tatiana, Pitcher, Toni, Tumas, Vitor, Luo, Wei, Zhou, Xiaopu, Tavadyan, Zaruhi

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Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians? von Sangare, Modibo, Dicko, Ilo, Guinto, Cheick Oumar, Sissoko, Adama, Dembele, Kekouta, Coulibaly, Youlouza, Coulibaly, Siaka Y., Landoure, Guida, Diallo, Abdallah, Dolo, Mamadou, Dolo, Housseini, Maiga, Boubacar, Traore, Moussa, Karembe, Mamadou, Traore, Kadiatou, Toure, Amadou, Sylla, Mariam, Togora, Arouna, Coulibaly, Souleymane, Traore, Sékou Fantamady, Hendrickson, Brant, Bricceno, Katherine, Schindler, Alice B., Kokkinis, Angela, Meilleur, Katherine G., Sangho, Hammadoun Ali, Diakite, Brehima, Kassogue, Yaya, Coulibaly, Yaya Ibrahim, Burnett, Barrington, Maiga, Youssoufa, Doumbia, Seydou, Fischbeck, Kenneth H.

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Diabetic polyneuropathy with/out neuropathic pain in Mali: A cross-sectional study in two reference diabetes treatment centers in Bamako von Maiga, Youssoufa, Diallo, Salimata, Konipo, Fatoumata dite Nènè, Sangho, Oumar, Sangare, Modibo, Diallo, Seybou H, Mahamadou, Saliou, Pereon, Yann, Giumelli, Bernard, Coulibaly, Awa, Daou, Mariam, Traore, Zoumana, Sow Sylla, Djeneba, Albakaye, Mohamed, Guinto, Cheick Oumar, Ouologem, Madani, Sissoko, Adama S, Traore, Hamar A, Coulibaly, Souleymane Papa, Damier, Philippe, Attal, Nadine, Nizard, Julien

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Genetics and genomic medicine in Mali: challenges and future perspectives von Landouré, Guida, Samassékou, Oumar, Traoré, Mahamadou, Meilleur, Katherine G., Guinto, Cheick Oumar, Burnett, Barrington G., Sumner, Charlotte J., Fischbeck, Kenneth H.

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Fibrodysplasia ossificans progressiva in a Malian boy of Bamako von Traore, Moussa, Traore Thomas, Jeannette, Guinto, Cheick Oumar, Kane, Mamady, Traore, Siona

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Type 2 Gaucher's disease in a Malian family von Traoré, Moussa, Sylla, Mariam, Traoré, Jeannette, Sidibé, Toumani, Oumar, Guinto Cheick

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Type 2 Gaucher\'s disease in a Malian family von Traoré, Moussa, Sylla, Mariam, Traoré, Jeannette, Sidibé, Toumani, Oumar, Guinto Cheick

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AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia von Diarra, Salimata, Ghosh, Saikat, Cissé, Lassana, Coulibaly, Thomas, Yalcouyé, Abdoulaye, Harmison, George, Diallo, Salimata, Diallo, Seybou H., Coulibaly, Oumar, Schindler, Alice, Cissé, Cheick A.K., Maiga, Alassane B., Bamba, Salia, Samassekou, Oumar, Khokha, Mustafa K., Mis, Emily K., Lakhani, Saquib A., Donovan, Frank X., Jacobson, Steve, Blackstone, Craig, Guinto, Cheick O., Landouré, Guida, Bonifacino, Juan S., Fischbeck, Kenneth H., Grunseich, Christopher

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A novel variant in the spatacsin gene causing SPG11 in a Malian family von Landouré, Guida, Dembélé, Kékouta, Diarra, Salimata, Cissé, Lassana, Samassékou, Oumar, Bocoum, Abdoulaye, Yalcouyé, Abdoulaye, Traoré, Moussa, Fischbeck, Kenneth H., Guinto, Cheick O.

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