Results 161 to 170 of about 1,607,316 (314)

Driving health system change in childhood cancer service delivery through multi-stakeholder engagement at state level – The Odisha experience

Pediatric Hematology Oncology Journal
Shivani Chauhan, Nitai Panigrahi, Saroj Panda, Rohini Pandey, Amarabati Mishra, Archisman Mohapatra, Ashwani Kumar Darjee, Haresh Gupta, Keshav Sharma, Madhulita Patnaik, Nabarun Panda, Nirmalya Deo Pradhan, Palash Das, Poonam Bagai, Prasanta Kumar Palatasingh, Sonali Mohapatra, Ramandeep Arora   +16 more
doaj   +1 more source

Exploring the Role of Alexithymia in the Relationship Between Childhood Trauma and Premenstrual Syndrome. [PDF]

Dev Psychobiol
Savoca PW, Ditzer J, Zietlow AL, Callaghan BL.   +3 more
europepmc   +1 more source

Investigating early childhood education for sustainability : insights from history and literature

, 2013
Seemingly straightforward tasks often have a way of becoming complex. This was the case for our guest editorial team charged with creating Early Childhood Australia’s Best of Sustainability publication drawn from the the Australasian Journal of Early ...
Davis, Julie M., Davis, Julie, Elliott, Sue   +2 more
core  

Neurological, Neurodevelopmental and Treatment Outcomes in Patients With Pyruvate Dehydrogenase Complex Deficiency

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The aim of this study was to characterize intellectual and motor function, neurological features including epilepsy, treatment response, and adaptive behavior in patients with pyruvate dehydrogenase complex deficiency (PDCD) in Sweden.
Antri Savvidou, Colin Reilly, Kalliopi Sofou, Sofia Ygberg, Erik A. Eklund, Karin Naess, Niklas Darin   +6 more
wiley   +1 more source

The association between habitual emotion regulation, childhood adversity, and cluster C personality disorders symptomatology. [PDF]

Front Psychol
Crişan ŞM, Miu AC, Szentágotai-Tătar A.   +2 more
europepmc   +1 more source

Nationwide Survey of Association Between Fever and Epileptic Seizure in CDKL5 Deficiency Disorder Revealed Therapeutic Implications

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective CDKL5 deficiency disorder (CDD) is a rare, severe developmental and epileptic encephalopathy. There is a pressing need to develop effective and sustainable therapeutic strategies. We aimed to investigate the causal association between febrile episodes and epileptic seizures for therapeutic implications in CDD patients.
Siyi Wang, Jialin Du, Jinghui Liu, Dongmei Hu, Hongxin Wang, Xiaoxiao Man, Lehong Gao, Shimin Hu, Xianghong Meng, Hongyang Zhao, Minjing Hu, Yingxue Yang, Zhiqi Xiong, Liankun Ren   +13 more
wiley   +1 more source

Drug safety alerts for childhood cancer medicines in India from CDSCO(2021-2025) and PvPI notifications (2016–2025)

Pediatric Hematology Oncology Journal
Rohini Pandey, Maharshi Trivedi, Haresh Gupta, Avinash Thumallapalli, Pooja Sharma, Ramandeep S. Arora   +5 more
doaj   +1 more source

Six decades of trends in BMI, thinness, overweight, and obesity among 210,927 Swedish children in different socioeconomic contexts. [PDF]

BMC Public Health
Bygdell M, Hemmed K, Martikainen J, Bonander C, Sjögren L, Ohlsson C, Kindblom JM.   +6 more
europepmc   +1 more source

Autoimmune Comorbidities as Modifiers of Phenotypic Heterogeneity in Facioscapulohumeral Dystrophy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral dystrophy type 1 (FSHD1) shows clinical heterogeneity that is only partly explained by D4Z4 repeat unit (RU) size. Although immune and inflammatory mechanisms may contribute to disease variability, the prevalence and clinical impact of autoimmune diseases in FSHD remain unclear.
Jonathan Pini, Giulia Tammam, Andra Ezaru, Manuela Gambella, Benoît Sanson, Luisa Villa, Michele Cavalli, Mihai‐Bogdan Ioncea, Angela Puma, Sabrina Sacconi   +9 more
wiley   +1 more source

A Novel KCNA1 Variant in a Patient With Tremor and Autism Spectrum Disorder Causes Mixed LOF/GOF Defects of Kv1.1 Channels

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Variants in KCNA1, encoding the Kv1.1 potassium channel, cause neurological disorders including episodic ataxia and developmental and epileptic encephalopathy. We identified a novel KCNA1 variant (A401T) in a 16‐year‐old patient with autism spectrum disorder, borderline intellectual disability, and tremor, without episodic ataxia or epilepsy ...
Juan Darío Ortigoza‐Escobar, Laura Marti‐Sánchez, Loreto Martorell, Giorgia Dinoi, Antonio Vittorio Buono, Annamaria De Luca, Antonella Liantonio, Paola Imbrici   +7 more
wiley   +1 more source