Results 171 to 180 of about 88,012 (270)

Reliability and accuracy of delirium assessments among investigators at multiple international centres [PDF]

, 2018
Avidan, Michael Simon, Escallier, Krisztina E, Inouye, Sharon K, Lin, Nan, Mashour, George A, Maybrier, Hannah R, Mickle, Angela M, Palihnich, Kerry, Hebrew SeniorLife, Boston, Scmitt, Eva M, Upadhyayula, Ravi T, Wildes, Troy S   +10 more
core   +1 more source

A novel in-frame deletion in KIF5C gene causes infantile onset epilepsy and psychomotor retardation. [PDF]

MedComm (2020)
Banerjee S, Zhao Q, Wang B, Qin J, Yuan X, Lou Z, Zheng W, Li H, Wang X, Cheng X, Zhu Y, Lin F, Yang F, Xu J, Munshi A, Das P, Zhou Y, Mandal K, Wang Y, Ayub M, Hirokawa N, Xi Y, Chen G, Li C.   +23 more
europepmc   +1 more source

Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN in-silico structural analysis. [PDF]

Front Genet
Vecchio D, Macchiaiolo M, Gonfiantini MV, Panfili FM, Petrizzelli F, Liorni N, Cortellessa F, Sinibaldi L, Rana I, Agolini E, Cocciadiferro D, Colantoni N, Semeraro M, Rizzo C, Deodati A, Cotugno N, Caggiano S, Verrillo E, Nucci CG, Alkan S, Saraiva JM, De Sá J, Almeida PM, Krishna J, Buonuomo PS, Martinelli D, Dionisi Vici C, Caputo V, Bartuli A, Novelli A, Mazza T.   +30 more
europepmc   +1 more source

Genetic Diagnostic Elucidation of a Patient With Multiorgan Granulomas, Facial Peculiarities, and Psychomotor Retardation. [PDF]

Front Genet, 2018
Soukup D, Kuechler A, Roesler J, Pichlmaier L, Eckerland M, Olivier M, Stehling F.   +6 more
europepmc   +1 more source

Autosomal Recessive Spastic Paraplegia and Psychomotor Retardation With or Without Seizures: A Case Report From Saudi Arabia. [PDF]

Cureus
Alzaidan H, Alluhaybi B, Albulayhid NA, Al-Jabr KH, Alotaibi FT, Alqahtani A.   +5 more
europepmc   +1 more source

First Case of Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation Harboring Co-inherited Variants in HERC1 and PMP22 Genes from Iran: Two Novel Variants. [PDF]

Arch Iran Med
Reshadmanesh A, Dehdahsi S, Ahangari F, Kahrizi K, Kariminejad A, Mahdavi SS, Talebi S, Najmabadi H.   +7 more
europepmc   +1 more source

A novel human Cdh1 mutation impairs anaphase promoting complex/cyclosome activity resulting in microcephaly, psychomotor retardation, and epilepsy. [PDF]

J Neurochem, 2019
Rodríguez C, Sánchez-Morán I, Álvarez S, Tirado P, Fernández-Mayoralas DM, Calleja-Pérez B, Almeida Á, Fernández-Jaén A.   +7 more
europepmc   +1 more source

Disrupted functional connectivity of the habenula links psychomotor retardation and deficit of verbal fluency and working memory in late-life depression. [PDF]

CNS Neurosci Ther
Su T, Chen B, Yang M, Wang Q, Zhou H, Zhang M, Wu Z, Lin G, Wang D, Li Y, Zhong X, Ning Y.   +11 more
europepmc   +1 more source

Correction to: Novel 1q22-q23.1 duplication in a patient with lambdoid and metopic craniosynostosis, muscular hypotonia, and psychomotor retardation. [PDF]

J Appl Genet, 2018
Sowińska-Seidler A, Olech EM, Socha M, Larysz D, Jamsheer A.   +4 more
europepmc   +1 more source

Psychomotor retardation in subtypes of depression

, 2006
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openaire   +1 more source