Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (6349)
All Articles published online
|
Publishing Process of This Article
|
Jan 26, 2019 (publication date) through Nov 23, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Nafi O, Ramadan B, Riess O, Buchert R, Froukh T. Two cases of variant late infantile ceroid lipofuscinosis in Jordan. World J Clin Cases 2019; 7(2): 203-208 [PMID: 30705896 DOI: 10.12998/wjcc.v7.i2.203] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v7/i2/203.htm |
| Number | Citing Articles |
| 1 |
Debaleena Mukherjee, Dwaipayan Bhattacharyya, Alak Pandit, Souvik Dubey. Higher order visual dysfunction and myoclonic-atonic seizure: an atypical presentation of CLN6 neuronal ceroid lipofuscinosis. BMJ Case Reports 2022; 15(2): e247790 doi: 10.1136/bcr-2021-247790
|
| 2 |
Tawfiq Froukh, Ammar Hawwari, Khalid Al Zubi. Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families. BMC Medical Genetics 2020; 21(1) doi: 10.1186/s12881-020-01112-z
|
| 3 |
R. Badilla-Porras, A. Echeverri-McCandless, J. M. Weimer, A. Ulate-Campos, A. Soto-Rodríguez, A. Gutiérrez-Mata, L. Hernández-Con, S. Bogantes-Ledezma, A. Balmaceda-Meza, J. Brudvig, A. Sanabria-Castro. Neuronal Ceroid Lipofuscinosis Type 6 (CLN6) clinical findings and molecular diagnosis: Costa Rica’s experience. Orphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-021-02162-z
|
| 4 |
Tawfiq Froukh, Omar Nafie, Sana' A. S. Al Hait, Lucia Laugwitz, Julia Sommerfeld, Marc Sturm, Aya Baraghiti, Tala Issa, Anis Al‐Nazer, Philipp A. Koch, Johannes Hanselmann, Beate Kootz, Peter Bauer, Wael Al‐Ameri, Rami Abou Jamra, Ayman J. Alfrook, Moath Hamadallah, Linda Sofan, Angelika Riess, Tobias B. Haack, Olaf Riess, Rebecca Buchert. Genetic basis of neurodevelopmental disorders in 103 Jordanian families. Clinical Genetics 2020; 97(4): 621 doi: 10.1111/cge.13720
|
| 5 |
Corina-Marcela Rus, Thomas Weissensteiner, Catarina Pereira, Iuliana Susnea, Bright D. Danquah, Galina Morales Torres, Maria Eugenia Rocha, Claudia Cozma, Deepa Saravanakumar, Sumanth Mannepalli, Krishna K. Kandaswamy, Sebastiano Di Bucchianico, Ralf Zimmermann, Arndt Rolfs, Peter Bauer, Christian Beetz. Clinical and genetic characterization of a cohort of 97 CLN6 patients tested at a single center. Orphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-022-02288-8
|
| 6 |
Mohammed M. Saleh, Abdulrahim M. Hamhom, Ali Al-Otaibi, Malak AlGhamdi, Yousef Housawi, Yaser I. Aljadhai, Seham Alameer, Mohammed Almannai, Lamyaa A. Jad, Ali H. Alwadei, Sadia Tabassum, Abdulaziz Alsaman, Ali AlAsmari, Fuad Al Mutairi, Hamad Althiyab, Fahad A. Bashiri, Suzan AlHumaidi, Majid Alfadhel, Jonathan W. Mink, Aqeela AlHashim, Eissa A. Faqeih, Amal Kentab, H.H. Muddathir, M.A. Salih, Aziza M. Mushiba, A.P. Zada, Mohammed S. Bamajboor, Sadique Zameer, Fahad AlBassam, Adel Mahmoud, A.A. Alnawfal, Mushari AlAmr, Maryam Bawazir, Ahmed Al Rumayyan, Waleed Al-Twaijri, Muhammed Talal Alrifai, Sumayah Al Hajjaj. Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia. Pediatric Neurology 2024; 155: 149 doi: 10.1016/j.pediatrneurol.2024.03.004
|