Intracranial tuberculoma and the challenges of global neurosurgery von Roy, Holly A, Cascini, Natasha, Ajay, Bini, Mukherjee, Sudipta, McGavin, Lucy, Inman, Alice, Wilkinson, Robert, Whitfield, Peter C

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SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission von Fasham, James, Huebner, Antje K, Liebmann, Lutz, Khalaf-Nazzal, Reham, Maroofian, Reza, Kryeziu, Nderim, Wortmann, Saskia B, Leslie, Joseph S, Ubeyratna, Nishanka, Mancini, Grazia M S, van Slegtenhorst, Marjon, Wilke, Martina, Haack, Tobias B, Shamseldin, Hanan E, Gleeson, Joseph G, Almuhaizea, Mohamed, Dweikat, Imad, Abu-Libdeh, Bassam, Daana, Muhannad, Zaki, Maha S, Wakeling, Matthew N, McGavin, Lucy, Turnpenny, Peter D, Alkuraya, Fowzan S, Houlden, Henry, Schlattmann, Peter, Kaila, Kai, Crosby, Andrew H, Baple, Emma L, Hübner, Christian A

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TECPR2‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine von Khalaf‐Nazzal, Reham, Dweikat, Imad, Ubeyratna, Nishanka, Fasham, James, Alawneh, Maysa, Leslie, Joseph, Maree, Mosab, Gunning, Adam, Zayed, Deyala Z., Voutsina, Nikol, McGavin, Lucy, Sawafta, Reem, Owens, Martina, Baker, Wisam, Turnpenny, Peter, Al‐Hijawi, Fida’, Baple, Emma L., Crosby, Andrew H., Rawlins, Lettie E.

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Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice von Rawlins, Lettie E, Almousa, Hashem, Khan, Shazia, Collins, Stephan C, Milev, Miroslav P, Leslie, Joseph, Saint-Dic, Djenann, Khan, Valeed, Hincapie, Ana Maria, Day, Jacob O, McGavin, Lucy, Rowley, Christine, Harlalka, Gaurav V, Vancollie, Valerie E, Ahmad, Wasim, Lelliott, Christopher J, Gul, Asma, Yalcin, Binnaz, Crosby, Andrew H, Sacher, Michael, Baple, Emma L

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Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency von Lin, Siying, Fasham, James, Al-Hijawi, Fida', Qutob, Nouar, Gunning, Adam, Leslie, Joseph S., McGavin, Lucy, Ubeyratna, Nishanka, Baker, Wisam, Zeid, Ramez, Turnpenny, Peter D., Crosby, Andrew H., Baple, Emma L., Khalaf-Nazzal, Reham

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Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder von Rawlins, Lettie E., Maroofian, Reza, Cannon, Stuart J., Daana, Muhannad, Zamani, Mina, Ghani, Shamsul, Leslie, Joseph S., Ubeyratna, Nishanka, Khan, Nasar, Khan, Hamid, Scardamaglia, Annarita, Cloarec, Robin, Khan, Shujaat Ali, Umair, Muhammad, Sadeghian, Saeid, Galehdari, Hamid, Al-Maawali, Almundher, Al-Kindi, Adila, Azizimalamiri, Reza, Shariati, Gholamreza, Ahmad, Faraz, Al-Futaisi, Amna, Rodriguez Cruz, Pedro M., Salazar-Villacorta, Ainara, Ndiaye, Moustapha, Diop, Amadou G., Sedaghat, Alireza, Saberi, Alihossein, Hamid, Mohammad, Zaki, Maha S., Vona, Barbara, Owrang, Daniel, Alhashem, Abdullah M., Obeid, Makram, Khan, Amjad, Beydoun, Ahmad, Najjar, Marwan, Tajsharghi, Homa, Zifarelli, Giovanni, Bauer, Peter, Hakami, Wejdan S., Al Hashem, Amal M., Boustany, Rose-Mary N., Burglen, Lydie, Alavi, Shahryar, Gunning, Adam C., Owens, Martina, Karimiani, Ehsan G., Gleeson, Joseph G., Milh, Mathieu, Salah, Somaya, Khan, Jahangir, Haucke, Volker, Wright, Caroline F., McGavin, Lucy, Elpeleg, Orly, Shabbir, Muhammad I., Houlden, Henry, Ebner, Michael, Baple, Emma L., Crosby, Andrew H.

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Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoform von Rickman, Olivia J., Salter, Claire G., Gunning, Adam C., Fasham, James, Voutsina, Nikol, Leslie, Joseph S., McGavin, Lucy, Cross, Harold E., Posey, Jennifer E., Akdemir, Zeynep Coban, Jhangiani, Shalini N., Lupski, James R., Baple, Emma L., Crosby, Andrew H.

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Motor Cortex Brain Activity Induced by 1-Hz Transcranial Magnetic Stimulation Is Similar in Location and Level to That for Volitional Movement von BOHNING, DARYL E, SHASTRI, ANANDA, McGAVIN, LUCY, McCONNELL, KATHLEEN A, NAHAS, ZIAD, LORBERBAUM, JEFFREY P, ROBERTS, DONNA R, GEORGE, MARK S

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SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission von Fasham, James, Huebner, Antje K, Liebmann, Lutz, Khalaf-Nazzal, Reham, Maroofian, Reza, Kryeziu, Nderim, Wortmann, Saskia B, Leslie, Joseph S, Ubeyratna, Nishanka, Mancini, Grazia MS, van Slegtenhorst, Marjon, Wilke, Martina, Haack, Tobias B, Shamseldin, Hanan, Gleeson, Joseph G, Almuhaizea, Mohamed, Dweikat, Imad, Abu-Libdeh, Bassam, Daana, Muhannad, Zaki, Maha S, Wakeling, Matthew N, McGavin, Lucy, Turnpenny, Peter D, Alkuraya, Fowzan S, Houlden, Henry, Schlattmann, Peter, Kaila, Kai, Crosby, Andrew H, Baple, Emma L, Hübner, Christian A

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Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice von Rawlins, Lettie E, Almousa, Hashem, Khan, Shazia, Collins, Stephan C, Milev, Miroslav P, Leslie, Joseph, Saint-Dic, Djenann, Khan, Valeed, Hincapie, Ana Maria, Day, Jacob O, McGavin, Lucy, Rowley, Christine, Harlalka, Gaurav V, Vancollie, Valerie E, Ahmad, Wasim, Lelliott, Christopher J, Gul, Asma, Yalcin, Binnaz, Crosby, Andrew H, Sacher, Michael, Baple, Emma L

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Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoform von Rickman, Olivia J, Salter, Claire G, Gunning, Adam C, Fasham, James, Voutsina, Nikol, Leslie, Joseph S, McGavin, Lucy, Cross, Harold E, Posey, Jennifer E, Akdemir, Zeynep Coban, Jhangiani, Shalini N, Lupski, James R, Baple, Emma L, Crosby, Andrew H

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