Wolfram Syndrome by J Gordon Millichap

Subjects: “…wolfram syndrome…”
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Wolfram syndrome: A rare case report by Anitha Padmanabhan, Aditi Parihar, Urmi S C. Vartak, Nitin M Gadgil

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Early presentation of gait impairment in Wolfram Syndrome by Pickett Kristen A, Duncan Ryan P, Hoekel James, Marshall Bess, Hershey Tamara, Earhart Gammon M

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Paediatric Wolfram syndrome Type 1: should gonadal dysfunction be part of the diagnostic criteria? by Giulio Frontino, Giulio Frontino, Raffaella Di Tonno, Raffaella Di Tonno, Marianna Rita Stancampiano, Marianna Rita Stancampiano, Francesca Arrigoni, Francesca Arrigoni, Andrea Rigamonti, Andrea Rigamonti, Elisa Morotti, Elisa Morotti, Daniele Canarutto, Daniele Canarutto, Riccardo Bonfanti, Riccardo Bonfanti, Riccardo Bonfanti, Gianni Russo, Graziano Barera, Lorenzo Piemonti, Lorenzo Piemonti

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A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report by Min Li, Jia Liu, Huan Yi, Li Xu, Xiufeng Zhong, Fuhua Peng

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A Case report of Wolfram Syndrome by Samaneh Norooziasl, Seyed Alireza Javadinia

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A pair of siblings with Wolfram Syndrome: a review of the literature and treatment options by Png, Doanna, Yeoh, Ester, Tan, Clara, Lim, Su Chi

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Sleep disturbances in Wolfram syndrome by Amy Licis, Gabriel Davis, Sarah A. Eisenstein, Heather M. Lugar, Tamara Hershey

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A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene by Jinhee Lee, Takuya Iwasaki, Tomoko Kaida, Hideki Chuman, Akiko Yoshimura, Yuji Okamoto, Hiroshi Takashima, Kazunori Miyata

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A deep phenotyping study in mouse and iPSC models to understand the role of oligodendroglia in optic neuropathy in Wolfram syndrome by K. Ahuja, M. Vandenabeele, F. Nami, E. Lefevere, J. Van hoecke, S. Bergmans, M. Claes, T. Vervliet, K. Neyrinck, T. Burg, D. De Herdt, P. Bhaskar, Y. Zhu, Z. J. Looser, J. Loncke, W. Gsell, M. Plaas, P. Agostinis, J. V. Swinnen, L. Van Den Bosch, G. Bultynck, A. S. Saab, E. Wolfs, Y. C. Chai, U. Himmelreich, C. Verfaillie, L. Moons, L. De Groef

Subjects: “…Wolfram syndrome…”
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Bilateral Optic Nerve Atrophy Case Report by Mohammed R. Naqeeb, Dina M Abdulmannan

Subjects: “…atrophy, optic nerve, wolfram syndrome, saudi arabia…”
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Thiamine– Responsive Megaloblastic Anemia Syndrome by F Motavaselian, F Nourani, Kh Dehghani, M Kheirandish, AH Jafari, A Hashemi

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Wolfram to Alstrom: Analysis of a Diagnostic Error by Annapoorna Chakrabarty, Shipra Rai, Kavitha Saravu

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Longitudinal hearing loss in Wolfram syndrome by Roanne Karzon, Anagha Narayanan, Ling Chen, Judith E. C. Lieu, Tamara Hershey

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Wolfram Syndrome in a Family with Variable Expression by Abdurrahman Kadayifci, Yalcin Kepekci, Yavuz Coskun, Ying Huang

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Multiomic analysis on human cell model of wolfram syndrome reveals changes in mitochondrial morphology and function by Agnieszka Zmyslowska, Miljan Kuljanin, Beata Malachowska, Marcin Stanczak, Dominika Michalek, Aneta Wlodarczyk, Dagmara Grot, Joanna Taha, Bartłomiej Pawlik, Magdalena Lebiedzińska-Arciszewska, Hanna Nieznanska, Mariusz R. Wieckowski, Piotr Rieske, Joseph D. Mancias, Maciej Borowiec, Wojciech Mlynarski, Wojciech Fendler

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Evaluation of pathogenic variant in WFS1 in a patient with Wolfram syndrome by Marziyeh Hoseinzadeh, Mohammad Mehdi Jahani, Samane Nasrniya, Mohammad Amin Tabatabaiefar

Subjects: “…Wolfram syndrome (WS)…”
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Wolfram Syndrome protein, Miner1, regulates sulphydryl redox status, the unfolded protein response, and Ca2+ homeostasis by Sandra E. Wiley, Alexander Y. Andreyev, Ajit S. Divakaruni, Robert Karisch, Guy Perkins, Estelle A. Wall, Peter van der Geer, Yi‐Fan Chen, Ting‐Fen Tsai, Melvin I. Simon, Benjamin G. Neel, Jack E. Dixon, Anne N. Murphy

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Taste and smell function in Wolfram syndrome by Raul Alfaro, Tasha Doty, Anagha Narayanan, Heather Lugar, Tamara Hershey, M. Yanina Pepino

Subjects: “…Wolfram syndrome…”
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Variable Expressivity of Wolfram Syndrome in a Family with Multiple Affected Subjects by Mehraban Mirrahimi, Sare Safi, Maryam Mohammadzadeh, Azadeh Doozandeh, Fatemeh Suri

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