Results 71 to 80 of about 48,040 (268)

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

Eating in eating disorders

, 2012
The aim of this paper is to bring eating back into the centre of the eating disorder discourse. The ability to interrogate and understand the central processes of appetite has increased considerably since the discovery of leptin and the ability to ...
Kan C., Cardi V., Treasure J.
core   +1 more source

Comparative Effectiveness and Safety of Inebilizumab Versus Rituximab in AQP4‐IgG‐Positive NMOSD

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Rituximab (anti‐CD20, RTX) and inebilizumab (anti‐CD19, INE) represent B‐cell‐depleting therapies used for aquaporin‐4 antibody‐positive (AQP4‐IgG+) neuromyelitis optica spectrum disorder (NMOSD); however, direct comparative evidence remains limited.
Jie Lin, Binbin Xue, Dewei Xie, Jia Li, Juyuan Pan, Lanbing Zhu, Qiaowen Tong, Jing Lin, Ruofan Zhu, Xu Zhang, Junhui Xia, Xiang Li   +11 more
wiley   +1 more source

Diagnostic Subtypes of Feeding Disorders in Infancy: An Empirical Contribution on Mother-Child Feeding Interactions, Child and Mother Psychopathological Risk Factors

, 2013
DIAGNOSTIC SUBTYPES OF FEEDING DISORDERS IN INFANCY: AN EMPIRICAL CONTRIBUTION ON MOTHER-CHILD FEEDING INTERACTIONS, CHILD AND MOTHER PSYCHOPATHOLOGICAL RISK FACTORS Introduction: DC:0-3, the manual of Mental Health and Developmental Disorders of ...
LUCARELLI, LOREDANA
core  

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

The role of family factors in eating disorders

, 2023
Historically, eating disorders have been considered as a product of disturbed inter-personal relationships, with a large focus on the role of families or family functioning.
Wonderlich, Steveeditor, Herpertz-Dahlmann, Beateeditor, Van Malderen, EvaPP070001104382378020024715160000-0002-4365-188839705D9A-F0EE-11E1-A9DE-61C894A0A6B4, Robinson, Pauleditor, Fernandez-Aranda, Fernandoeditor, Treasure, Janeteditor, Goossens, LienPP070019993076188010018379060000-0002-5518-2855F70F6522-F0ED-11E1-A9DE-61C894A0A6B4, De Coen, JolienUGent0001105811118020033753339735171410830000-0002-6582-4006369ED3E4-F0EE-11E1-A9DE-61C894A0A6B4, Taquet, JuliettePP070001005460558020033809890000-0002-5253-92222D409A08-F0EE-11E1-A9DE-61C894A0A6B4, Wade, Traceyeditor   +9 more
core  

Psychotherapies for eating disorders : findings from a rapid review

, 2023
Background: Psychotherapy is considered central to the effective treatment of eating disorders—focusing on behavioural, psychological, and social factors that contribute to the illness.
Hart, M., Maguire, S., Paterson, R., Bryant, E., Russell, J., Spielman, K., Vartanian, L., Miskovic-Wheatley, J., Singh, U., Wallis, A., Long, R., McLean, S., Mitchison, Deborah (R17748), Vatter, S., Marks, P., Hay, Phillipa (R12066), Raykos, B., Dzajkovski, N., Phillipou, A., Kohn, M., Wells, S., O’Kearney, R., King, R., Touyz, S., Thomson, J., Calvert, S., Koreshe, E., Ward, W., Clarke, S., Kay-Lambkin, F., Griffin, K., Smith, S., Williams, M., Utpala, R., Barakat, S., Hambleton, A., Krug, I., Dammery, G., Brennan, L., Chiem, L., Boakes, R., Long, A., Russell, H., Carroll, B., Tiggemann, M., Hickie, I., Foroughi, Nasim (R18162), Wilksch, S., Maloney, D., Aouad, P., Rhodes, P., Fursland, A., Gonzalez-Arce, V., Shelton, B., Le, A., Gouldthorp, B., Fuller-Tyszkiewicz, M., Caldwell, B., Pinkus, R., Chelius, B., Paxton, S., Fardouly, J., Smith, Evelyn (R18110), Conti, Janet E. (R18118), Pepin, G., Feneley, J., Hart, S., Rockett, K., Sawyer, S., Hannigan, A., Ong, S.H., Caterson, I., Rodan, S., Rieger, E., Madden, S., Piccone, J., Meddick, T., Wertheim, E., Linardon, J., Byrne, S., Griffiths, S., Castle, D., Crouch, L., Salter, F., Squire, S., Pehlivan, M.   +85 more
core   +1 more source

Onasemnogene Abeparvovec in Patients With SMA: Interim Results of the RESTORE Registry in Japan

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective There are limited real‐world data regarding the safety and effectiveness of onasemnogene abeparvovec (OA; Zolgensma) infusion, a one‐time gene replacement therapy, for Japanese patients with spinal muscular atrophy (SMA). We aimed to improve understanding of the real‐world outcomes for OA in Japan.
Kayoko Saito, Kamal Benguerba, Ken Tsuchida, Kazushige Yazawa, Isao Tsumiyama, Hiromitsu Kayama, Sandra P. Reyna, Farid Khan, Richard S. Finkel   +8 more
wiley   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source

Mothers’ eating disorder history and mother and infant attention to food during infant meal times: a candidate for intergenerational transmission of eating disorder behaviours

Frontiers in Child and Adolescent Psychiatry
IntroductionThere is evidence to suggest that individuals with eating disorders (EDs) show differences in attention to food compared to those without eating disorders.
Fay Huntley, Rebecca M. Pearson, Ilaria Costantini, Ilaria Costantini, Marc H. Bornstein, Marc H. Bornstein, Amy Campbell, Amy Campbell, Amy Campbell, Amy Campbell, Miguel Cordero, Nicky Wright   +11 more
doaj   +1 more source