Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders

Authors: Cali, Elisa ¹, Quirin, Tania ², Rocca, Clarissa ¹, Efthymiou, Stephanie ¹, Riva, Antonella ³, Marafi, Dana ^{4, 5}, Zaki, Maha S. ⁶, Suri, Mohnish ^{7, 8}, Dominguez, Roberto ⁹, Elbendary, Hasnaa M. ⁶, Alavi, Shahryar ^{1, 10}, Abdel-Hamid, Mohamed S. ¹¹, Morsy, Heba ^{1, 12}, Mau-Them, Frederic Tran ^{13, 14}, Nizon, Mathilde ^{15, 16}, Tesner, Pavel ¹⁷, Ryba, Lukáš ¹⁷, Zafar, Faisal ¹⁸, Rana, Nuzhat ¹⁸, Saadi, Nebal W. ¹⁹, Firoozfar, Zahra ¹⁰, Gencpinar, Pinar ²⁰, Unay, Bulent ²¹, Ustun, Canan ²¹, Bruel, Ange-Line ^{22, 23}, Coubes, Christine ²⁴, Stefanich, Jennifer ²⁵, Sezer, Ozlem ²⁶, Agolini, Emanuele ²⁷, Novelli, Antonio ²⁷, Vasco, Gessica ²⁸, Lettori, Donatella ²⁸, Milh, Mathieu ²⁹, Villard, Laurent ³⁰, Zeidler, Shimriet ³¹, Opperman, Henry ³², Strehlow, Vincent ³², Issa, Mahmoud Y. ⁶, El Khassab, Hebatallah ³³, Chand, Prem ³⁴, Ibrahim, Shahnaz ³⁴, Rashidi-Nezhad, Ali ^{35, 36}, Miryounesi, Mohammad ³⁷, Larki, Pegah ³⁷, Morrison, Jennifer ³⁸, Cristian, Ingrid ³⁸, Thiffault, Isabelle ^{39, 40, 41}, Bertsch, Nicole L. ⁴², Noh, Grace J. ⁴³, Pappas, John ^{44, 45}, Moran, Ellen ⁴⁶, Marinakis, Nikolaos M. ⁴⁷, Traeger-Synodinos, Joanne ⁴⁷, Hosseini, Susan ⁴⁸, Abbaszadegan, Mohammad Reza ⁴⁹, Caumes, Roseline ⁵⁰, Vissers, Lisenka E.L.M. ^{51, 52}, Neshatdoust, Maedeh ⁵³, Montazer Zohour, Mostafa ⁵⁴, El Fahime, Elmostafa ⁵⁵, Canavati, Christina ⁵⁶, Kamal, Lara ⁵⁶, Kanaan, Moien ⁵⁶, Askander, Omar ⁵⁷, Voinova, Victoria ^{58, 59}, Levchenko, Olga ⁶⁰, Haider, Shahzhad ⁶¹, Halbach, Sara S. ⁶², Elias Maia, Rayana ⁶³, Mansoor, Salehi ^{64, 65}, Jain, Vivek ⁶⁶, Tawde, Sanjukta ⁶⁷, Challa, Viveka Santhosh R. ⁶⁸, Gowda, Vykuntaraju K. ⁶⁸, Srinivasan, Varunvenkat M. ⁶⁸, Victor, Lucas Alves ⁶⁹, Pinero-Banos, Benito ⁷⁰, Hague, Jennifer ⁷¹, ElAwady, Heba Ahmed ⁷², Maria de Miranda Henriques-Souza, Adelia ⁷³, Cheema, Huma Arshad ⁷⁴, Anjum, Muhammad Nadeem ⁷⁴, Idkaidak, Sara ⁷⁵, Alqarajeh, Firas ⁷⁶, Atawneh, Osama ⁷⁶, Mor-Shaked, Hagar ⁷⁷, Harel, Tamar ⁷⁷, Zifarelli, Giovanni ⁷⁸, Bauer, Peter ⁷⁸, Kok, Fernando ⁷⁹, Kitajima, Joao Paulo ⁷⁹, Monteiro, Fabiola ⁷⁹, Josahkian, Juliana ⁷⁹, Lesca, Gaetan ^{80, 81}, Chatron, Nicolas ^{80, 81}, Ville, Dorothe ⁸², Murphy, David ⁸³, Neul, Jeffrey L. ⁸⁴, Mullegama, Sureni V. ⁸⁵, Begtrup, Amber ⁸⁵, Herman, Isabella ⁸⁶, Mitani, Tadahiro ⁴, Posey, Jennifer E. ⁴, Tay, Chee Geap ⁸⁷, Javed, Iram ⁸⁸, Carr, Lucinda ⁸⁹, Kanani, Farah ⁹⁰, Beecroft, Fiona ⁹⁰, Hane, Lee ⁹¹, Abdelkreem, Elsayed ⁹², Macek, Milan ¹⁷, Bispo, Luciana ⁹³, Elmaksoud, Marwa Abd ⁹⁴, Hashemi-Gorji, Farzad ⁹⁵, Pehlivan, Davut ^{4, 86}, Amor, David J. ⁹⁶, Jamra, Rami Abou ³², Chung, Wendy K. ⁹⁷, Ghayoor Karimiani, Eshan ^{98, 99, 100}, Campeau, Philippe M. ^{101, 102}, Alkuraya, Fowzan S. ¹⁰³, Pagnamenta, Alistair T. ¹⁰⁴, Gleeson, Joseph G. ^{105, 106}, Lupski, James R. ^{4, 107, 108}, Striano, Pasquale ^{3, 109}, Moreno-De-Luca, Andres ¹¹⁰, Lafontaine, Denis L.J. ², Houlden, Henry ¹, Maroofian, Reza ^{1, ∗}

Source: In Genetics in Medicine September 2024

The spectrum of hereditary neuromuscular disorders in the Pakistani population

Authors: Akbar, Fizza, Saleem, Shafaq Muhammad, Khalid, Ehtesham, Ibrahim, Shahnaz, Afroze, Bushra, Kirmani, Salman, Khan, Sara

Source: American journal of medical genetics.Part A. 191(10):2536-2550

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100192929054.0x000001&indx=1&recIds=ETOCvdc_100192929054.0x000001

Challenging the assumptions of social entrepreneurship education and repositioning it for the future: wonders of cultural, social, symbolic and economic capitals

Authors: Karatas-Ozkan, Mine, Ibrahim, Shahnaz, Ozbilgin, Mustafa, Fayolle, Alain, Manville, Graham, Nicolopoulou, Katerina, Tatli, Ahu, Tunalioglu, Melike

Source: Social enterprise journal. 19(2):98-122

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100179103895.0x000001&indx=1&recIds=ETOCvdc_100179103895.0x000001

Spectrum of Common Pediatric Neurological Disorders: A Cross-Sectional Study From Three Tertiary Care Centres Across Pakistan

Authors: Chand, Prem, Sultan, Tipu, Kulsoom, Shazia, Jan, Farida, Ibrahim, Shahnaz, Mukhtiar, Khairunnisa, Awan, Safia, Rafique, Ibrar, Khan, Durray Shahwar A., Sulaiman, Asna, Saqib, Muhammad Arif Nadeem, Sajid, Muhammad, Padhani, Zahra Ali, Das, Jai K., Soomro, Shazia, Wasay, Mohammad

Source: Pediatric neurology. 138:33-37

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100178467463.0x000001&indx=1&recIds=ETOCvdc_100178467463.0x000001

Dual nature of the relationship between corporate social responsibility and human resource management: A blessing or a curse?

Authors: Karatas‐Ozkan, Mine, Özgören, Çağla, Yamak, Sibel, Ibrahim, Shahnaz, Tunalıoğlu, Melike Nur, Pinnington, Ashly, Nicolopoulou, Katerina, Baruch, Yehuda

Source: Corporate social responsibility and environmental management. 29(5):1578-1594

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100159884576.0x000001&indx=1&recIds=ETOCvdc_100159884576.0x000001

Utility of genetic testing in pediatric epilepsy: Experience from a low to middle-income country

Authors: Akbar, Fizza, Saleh, Raisa, Kirmani, Salman, Chand, Prem, Mukhtiar, Khairunnisa, Jan, Farida, Kumar, Raman, Ibrahim, Shahnaz

Source: In Epilepsy & Behavior Reports 2022 20

PIGG variant pathogenicity assessment reveals characteristic features within 19 families

Authors: Tremblay-Laganière, Camille, Maroofian, Reza, Nguyen, Thi Tuyet Mai, Karimiani, Ehsan Ghayoor, Kirmani, Salman, Akbar, Fizza, Ibrahim, Shahnaz, Afroze, Bushra, Doosti, Mohammad, Ashrafzadeh, Farah, Babaei, Meisam, Efthymiou, Stephanie, Christoforou, Marilena, Sultan, Tipu, Ladda, Roger L., McLaughlin, Heather M., Truty, Rebecca, Mahida, Sonal, Cohen, Julie S., Baranano, Kristin, Ismail, Fatima Y., Patel, Millan S., Lehman, Anna, Edmondson, Andrew C., Nagy, Amanda, Walker, Melissa A., Mercimek-Andrews, Saadet, Maki, Yuta, Sachdev, Rani, Macintosh, Rebecca, Palmer, Elizabeth E., Mancini, Grazia M.S., Barakat, Tahsin Stefan, Steinfeld, Robert, Rüsch, Christina T., Stettner, Georg M., Wagner, Matias, Wortmann, Saskia B., Kini, Usha, Brady, Angela F., Stals, Karen L., Ismayilova, Naila, Ellard, Sian, Bernardo, Danilo, Nugent, Kimberly, McLean, Scott D., Antonarakis, Stylianos E., Houlden, Henry, Kinoshita, Taroh, Campeau, Philippe M., Murakami, Yoshiko

Source: In Genetics in Medicine October 2021 23(10):1873-1881

Clinical, neuroimaging, and molecular spectrum of TECPR2‐associated hereditary sensory and autonomic neuropathy with intellectual disability

Authors: Neuser, Sonja, Brechmann, Barbara, Heimer, Gali, Brösse, Ines, Schubert, Susanna, O'Grady, Lauren, Zech, Michael, Srivastava, Siddharth, Sweetser, David A., Dincer, Yasemin, Mall, Volker, Winkelmann, Juliane, Behrends, Christian, Darras, Basil T., Graham, Robert J., Jayakar, Parul, Byrne, Barry, Bar‐Aluma, Bat El, Haberman, Yael, Szeinberg, Amir, Aldhalaan, Hesham M., Hashem, Mais, Al Tenaiji, Amal, Ismayl, Omar, Al Nuaimi, Asma E., Maher, Karima, Ibrahim, Shahnaz, Khan, Fatima, Houlden, Henry, Ramakumaran, Vijayalakshmi S., Pagnamenta, Alistair T., Posey, Jennifer E., Lupski, James R., Tan, Wen‐Hann, ElGhazali, Gehad, Herman, Isabella, Muñoz, Tatiana, Repetto, Gabriela M., Seitz, Angelika, Krumbiegel, Mandy, Poli, Maria Cecilia, Kini, Usha, Efthymiou, Stephanie, Meiler, Jens, Maroofian, Reza, Alkuraya, Fowzan S., Abou Jamra, Rami, Popp, Bernt, Ben‐Zeev, Bruria, Ebrahimi‐Fakhari, Darius

Source: Human mutation. 42(6):762-776

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100121065541.0x000001&indx=1&recIds=ETOCvdc_100121065541.0x000001

Atypical presentation of biotinidase deficiency: masquerading neuromyelitis optica spectrum disorder.

Authors: Ali, Farhan, Mukhtiar, Khairunnisa, Raza, Mohammad, Ibrahim, Shahnaz

Source: BMJ Case Reports; Jul2024, Vol. 17 Issue 7, p1-4, 4p

MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study

Authors: Ansar, Zeeshan, Nasir, Asghar, Moatter, Tariq, Khan, Sara, Kirmani, Salman, Ibrahim, Shahnaz, Imam, Kahkashan, Ather, Anif, Samreen, Azra, Hasan, Zahra

Source: Genetic testing and molecular biomarkers. 23(7):468-472

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100084584586.0x000001&indx=1&recIds=ETOCvdc_100084584586.0x000001

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

Authors: Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba‐Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D., Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E. C., Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J. R., Wood, Nicholas W., Rothman, James E., Boycott, Kym M., Mills, Philippa B., Clayton, Peter T., Houlden, Henry, Kriouile, Yamna, Khorassani, Mohamed El, Aguennouz, Mhammed, Groppa, Stanislav, Marinova Karashova, Blagovesta, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez‐Dueñas, Belen, Di Rosa, Gabriella, Goraya, Jatinder S., Sultan, Tipu, Mine, Jun, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Banu, Selina, Pineda‐Marfa, Mercedes, Veggiotti, Pierangelo, Ferrari, Michel D., van den Maagdenberg, Arn M J M, Verrotti, Alberto, Marseglia, Giangluigi, Savasta, Salvatore, García‐Silva, Mayte, Ruiz, Alfons Macaya, Garavaglia, Barbara, Borgione, Eugenia, Portaro, Simona, Sanchez, Benigno Monteagudo, Boles, Richard, Papacostas, Savvas, Vikelis, Michail, Rothman, James, Giunti, Paola, Salpietro, Vincenzo, Oconnor, Emer, Kullmann, Dimitri, Kaiyrzhanov, Rauan, Sullivan, Roisin, Khan, Alaa Matooq, Yau, Wai Yan, Hostettler, Isabel, Papanicolaou, Eleni Zamba, Dardiotis, Efthymios, Maqbool, Shazia, Ibrahim, Shahnaz, Kirmani, Salman, Rana, Nuzhat Noureen, Atawneh, Osama, Lim, Shen‐Yang, Shaikh, Farooq, Koutsis, George, Breza, Marianthi, Mangano, Salvatore, Scuderi, Carmela, Morello, Giovanna, Stojkovic, Tanya, Torti, Erin, Zollo, Massimi, Heimer, Gali, Dauvilliers, Yves A., Striano, Pasquale, Al‐Khawaja, Issam, Al‐Mutairi, Fuad, Alkuraya, Fowzan S, Sherifa, Hamed, Rizig, Mie, Okubadejo, Njideka U., Ojo, Oluwadamilola O., Oshinaike, Olajumoke O., Wahab, Kolawole, Bello, Abiodun H., Abubakar, Sanni, Obiabo, Yahaya, Nwazor, Ernest, Ekenze, Oluchi, Williams, Uduak, Iyagba, Alagoma, Taiwo, Lolade, Komolafe, Morenikeji, Oguntunde, Olapeju, Pchelina, Sofya, Senkevich, Konstantin, Haridy, Nourelhoda, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Manizha, Ganieva, Isrofilov, Maksud, Guliyeva, Ulviyya, Salayev, Kamran, Khachatryan, Samson, Rossi, Salvatore, Silvestri, Gabriella, Bourinaris, Thomas, Xiromerisiou, Georgia, Fidani, Liana, Spanaki, Cleanthe, Tucci, Arianna

Source: Annals of neurology. 86(2):225-240

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100086949060.0x000001&indx=1&recIds=ETOCvdc_100086949060.0x000001

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

Authors: Hannah, Michael G., Bugiardini, Enrico, Bertini, Enrico, Kriouile, Yamna, El-Khorassani, Mohamed, Aguennouz, Mhammed, Groppa, Stanislav, Karashova, Blagovesta M., Goraya, Jatinder S., Sultan, Tipu, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Banu, Selina, Veggiotti, Pierangelo, Verrotti, Alberto, Lanari, Marcello, Savasta, Salvatore, Macaya, Alfons, Garavaglia, Barbara, Borgione, Eugenia, Papacostas, Savvas, Vikelis, Michail, Chelban, Viorica, Kaiyrzhanov, Rauan, Cortese, Andrea, Sullivan, Roisin, Papanicolaou, Eleni Z., Dardiotis, Efthymios, Maqbool, Shazia, Ibrahim, Shahnaz, Kirmani, Salman, Rana, Nuzhat N., Atawneh, Osama, Lim, Shen-Yang, Zuccotti, Gian V., Marseglia, Gian L., Esposito, Susanna, Shaikh, Farooq, Cogo, Paola, Corsello, Giovanni, Mangano, Salvatore, Nardello, Rosaria, Mangano, Donato, Scardamaglia, Annarita, Koutsis, George, Scuderi, Carmela, Ferrara, Pietro, Morello, Giovanna, Zollo, Massimo, Berni-Canani, Roberto, Terracciano, Luigi M., Sisto, Antonio, Di Fabio, Sandra, Strano, Federica, Scorrano, Giovanna, Di Bella, Saverio, Di Francesco, Ludovica, Manizha, Ganieva, Isrofilov, Maksud, Guliyeva, Ulviyya, Salayev, Kamran, Khachatryan, Samson, Xiromerisiou, Georgia, Spanaki, Cleanthe, Fiorillo, Chiara, Iacomino, Michele, Gaudio, Eugenio, Munell, Francina, Gagliano, Antonella, Jan, Farida, Chimenz, Roberto, Gitto, Eloisa, Iughetti, Lorenzo, Di Rosa, Gabriella, Maghnie, Mohamad, Pettoello-Mantovani, Massimo, Gupta, Neerja, Kabra, Madhulika, Benrhouma, Hanene, Tazir, Meriem, Bottone, Gabriella, Farello, Giovanni, Delvecchio, Maurizio, Di-Donato, Giulio, Obeid, Makram, Bakhtadze, Sophia, Saadi, Nebal W., Miraglia-Del-Giudice, Michele, Maccarone, Rita, Zaki, Maha S., Triki, Chahnez C., Kara, Majdi, Karimiani, Ehsan G., Salih, Ahmed M., Ramenghi, Luca A., Seri, Marco, Di-Falco, Giovanna, Mandarà, Luana, Barrano, Giuseppe, Elisa, Maurizio, Cherubini, Enrico, Operto, Francesca F., Valenzise, Mariella, Cattaneo, Antonino, Zazzeroni, Francesca, Alesse, Edoardo, Matricardi, Sara, Zafar, Faisal, Ullah, Ehsan, Afzal, Erum, Rahman, Fatima, Ahmed, Muhammad M., Parisi, Pasquale, Spalice, Alberto, De Filippo, Maria, Licari, Amelia, Trebbi, Edoardo, Romano, Ferdinando, Heimer, Gali, Al-Khawaja, Issam, Al-Mutairi, Fuad, Alkuraya, Fowzan S., Rizig, Mie, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Salpietro, Vincenzo, Maroofian, Reza, Wangen, Jamie, Ciolfi, Andrea, Barresi, Sabina, Efthymiou, Stephanie, Lamaze, Angelique, Aughey, Gabriel N., Al Mutairi, Fuad, Rad, Aboulfazl, Rocca, Clarissa, Calì, Elisa, Accogli, Andrea, Zara, Federico, Striano, Pasquale, Mojarrad, Majid, Tariq, Huma, Giacopuzzi, Edoardo, Taylor, Jenny C., Oprea, Gabriela, Skrahina, Volha, Rehman, Khalil Ur, Abd Elmaksoud, Marwa, Bassiony, Mahmoud, El Said, Huda G., Abdel-Hamid, Mohamed S., Al Shalan, Maha, Seo, Gohun, Kim, Sohyun, Lee, Hane, Khang, Rin, Issa, Mahmoud Y., Elbendary, Hasnaa M., Rafat, Karima, Marinakis, Nikolaos M., Traeger-Synodinos, Joanne, Ververi, Athina, Sourmpi, Mara, Eslahi, Atieh, Khadivi Zand, Farhad, Beiraghi Toosi, Mehran, Babaei, Meisam, Jackson, Adam, Bertoli-Avella, Aida, Pagnamenta, Alistair T., Niceta, Marcello, Battini, Roberta, Corsello, Antonio, Leoni, Chiara, Chiarelli, Francesco, Dallapiccola, Bruno, Faqeih, Eissa Ali, Tallur, Krishnaraya K., Alfadhel, Majid, Alobeid, Eman, Maddirevula, Sateesh, Mankad, Kshitij, Banka, Siddharth, Ghayoor-Karimiani, Ehsan, Tartaglia, Marco, Chung, Wendy K., Green, Rachel, Jepson, James E.C., Houlden, Henry

Source: In The American Journal of Human Genetics 4 January 2024 111(1):200-210

CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani children

Authors: Ibrahim, Shahnaz, Maqbool, Saadia, Azam, Maleeha, Iqbal, Mohammad Perwaiz, Qamar, Raheel

Source: MOLECULAR BIOLOGY REPORTS. 45(3):353-360

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100118600019.0x000001&indx=1&recIds=ETOCvdc_100118600019.0x000001

Infantile Spasms: Clinical profile and treatment outcomes

Authors: Kulsoom, Shazia, Ibrahim, Shahnaz H., Jafri, Sidra Kaleem, Moorani, Khemchand N., Anjum, Misbah

Source: Pakistan journal of medical sciences. 34(6):1424-1428

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN618290759&indx=1&recIds=ETOCRN618290759

Clinical Spectrum, Treatment and Outcome of Children with Autoimmune Encephalitis.

Authors: Raza, Mohammad, Mukhtiar, Khairunnisa, Ibrahim, Shahnaz

Source: Journal of the College of Physicians & Surgeons Pakistan; Mar2024, Vol. 34 Issue 3, p323-328, 6p

Actioning sustainability through tourism entrepreneurship: Women entrepreneurs as change agents navigating through the field of stakeholders.

Authors: Karatas-Ozkan, Mine, Tunalioglu, Renan, Ibrahim, Shahnaz, Ozeren, Emir, Grinevich, Vadim, Kimaro, Joseph

Source: Central European Management Journal; 2024, Vol. 32 Issue 1, p31-56, 26p

Subject Terms: BUSINESSWOMEN, SUSTAINABLE tourism, SUSTAINABILITY, SUSTAINABLE development, GENDER role, ENTREPRENEURSHIP, CHANGE agents

Geographic Terms: TURKEY

Company/Entity: UNITED Nations

Spectrum of MRI brain findings in subacute sclerosing panencephalitis

Authors: Jafri, Sidra, Husen, Yousuf, Ahmed, Khalid, Ibrahim, Shahnaz

Source: Asia pacific journal of clinical trials. 2(4):124-128

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100088343149.0x000001&indx=1&recIds=ETOCvdc_100088343149.0x000001

Description of Guillain-Barre syndrome on the basis of clinical features using Hughes scoring system among children in Karachi, Pakistan

Authors: Chand, Prem, Jan, Farida, Kaleem, Sidra, Yousafzai, Mohammad, Ibrahim, Shahnaz

Source: Asia pacific journal of clinical trials. 2(2):45-49

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100088343077.0x000001&indx=1&recIds=ETOCvdc_100088343077.0x000001

P097: Clinical whole genome sequencing for a highly consanguineous population in low-resource settings: Experience from an academic medical center in Pakistan

Authors: Akbar, Fizza, Mehboobali, Arif, Hasan, Zohra, Kaleem, Sidra, Ibrahim, Shahnaz, Kirmani, Salman

Source: In Genetics in Medicine Open 2023 1(1) Supplement

Diagnostic dilemmas and challenges in the management of myasthenia in infants and toddlers: A case report.

Authors: Mukhtiar, Khairunnisa, Raza, Mohammad, Tejani, Isbaah, Ali, Farhan, Ibrahim, Shahnaz

Source: SAGE Open Medical Case Reports; 11/7/2023, p1-6, 6p