Results 101 to 110 of about 777,243 (151)

Pseudoptosis due to acute dacryoadenitis: An unusual presentation of Epstein-Barr virus infection in a child. [PDF]

J Family Med Prim Care
Alotaibi F, Alshehri Z, Hameed T.
europepmc   +1 more source

Sustainability in Early Childhood: Almost mainstream: Re-imagining early childhood education for sustainable futures

, 2023
Davis, Julie, Elliott, Sue, https://orcid.org/   +2 more
core  

Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko's Lines in an Elderly Patient: A Rare Presentation. [PDF]

Indian J Dermatol
Mishra P, Sahoo S, Hota SK, Mohanty L, Dash S, Senapati A.   +5 more
europepmc   +1 more source

Mouse Model of Fast-Channel Genetic Myasthenic Syndrome Carrying <i>Chrne</i> p.P141L Mutation. [PDF]

Biomolecules
Webster RG, Maxwell S, Dong YY.
europepmc   +1 more source

Myasthenia Gravis in Pregnancy: Prenatal and Postnatal Diagnostic Challenges-A Narrative Review. [PDF]

Diagnostics (Basel)
Gerede A, Danavasi M, Oikonomou E, Papasozomenou P, Kourti V, Potiris A, Chatzakis C, Stavros S, Koutlaki N, Eleftheriadis M.   +9 more
europepmc   +1 more source

ALG14 variants contribute to a congenital disorder of glycosylation characterized by congenital myasthenia and epilepsy. [PDF]

HGG Adv
Marquez J, Rouxel F, It FE, Couturier V, Duplomb L, Bourgeois V, Briffaut AS, Bruel AL, Chevarin M, Ganne B, Ng BG, Viviano S, Hektor MPN, Pasha RA, Gatinois V, Larrieu-Arguille C, Faure JM, Prodhomme O, Colmard M, Rivier F, Yukimune O, Poe C, Rouvet I, Vitobello A, Thauvin C, Rodriguez-Gomez GD, Tolusso LK, Katata Y, Kikuchi A, Hoffman TL, Andersson HC, Deniz E, He M, Wells CF, Denommé-Pichon AS, Edmondson AC, Freeze HH, Lam C.   +37 more
europepmc   +1 more source

Identification of Ocular and Systemic Predictors and Development of a Prediction Model in Ocular Myasthenia Gravis. [PDF]

Transl Vis Sci Technol
Cai Y, Tang T, Peng S, Gong D, Zhang R, Zhou Q.   +5 more
europepmc   +1 more source

Slow-Channel Congenital Myasthenic Syndrome Due to <i>CHRND</i> Mutation in South Korea. [PDF]

J Clin Neurol
Min JH, Sohn SY, Kim SY, Joo IS.
europepmc   +1 more source

Phenotypic Diversity in Pediatric Congenital Myasthenic Syndrome: Insights from CHRNE and DPAGT1 Variants. [PDF]

Neurol Int
Ewida A, Al-Qaimari D, Shah U, Sudarsan N.   +3 more
europepmc   +1 more source