Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Karen H. Harum"'
Publikováno v:
Developmental Medicine & Child Neurology. 41:781-785
Inherited and acquired thrombophilic disorders have recently been associated with cerebral palsy (CP) and complications in pregnancy. Thrombophilic disorders are not diseases per se, but are recognized risk factors for a variety of diseases across al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68fb6cb7339a57e8253302e328010be4
https://doi.org/10.1111/j.1469-8749.1999.tb00539.x
https://doi.org/10.1111/j.1469-8749.1999.tb00539.x
Publikováno v:
Pediatric Research. 53:369-374
Cognitive disorders in children have traditionally been described in terms of clinical phenotypes or syndromes, chromosomal lesions, metabolic disorders, or neuropathology. Relatively little is known about how these disorders affect the chemical reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ac9a109fa7ff74ae8508cde36973d45
https://doi.org/10.1203/01.pdr.0000049517.47493.e9
https://doi.org/10.1203/01.pdr.0000049517.47493.e9
Publikováno v:
Neurology. 56:207-214
Background: Gene expression and protein synthesis, mediated by the transcription factor CREB (cAMP response element binding protein), play an important role in learning and memory in several species, including Drosophila , snails, and mice. Patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec08869fb3fddab366667892845cd0de
https://doi.org/10.1212/wnl.56.2.207
https://doi.org/10.1212/wnl.56.2.207
Publikováno v:
Journal of Applied Social Psychology. 29:2308-2327
The present studies were designed to evaluate methodological influences on the efficiency of genetic-screening studies, specifically when enrolling preschoolers in a prevalence study of the fragile X full mutation. The studies include replication of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf052cf8ed54d787e828281127cbfa4e
https://doi.org/10.1111/j.1559-1816.1999.tb00112.x
https://doi.org/10.1111/j.1559-1816.1999.tb00112.x
Autor:
Michael V. Johnston, Karen H. Harum
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 20:50-56
Memory, the ability to store and retrieve information, is essential for learning in children. Modern neurobiology research is revealing some of the fundamental steps that encode memories within networks of neuronal synaptic connections in the brain.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9470774b545a54e079b983d1f0fb4af3
https://doi.org/10.1097/00004703-199902000-00009
https://doi.org/10.1097/00004703-199902000-00009
Autor:
Michael V. Johnston, Karen H Harum
Publikováno v:
Mental Retardation and Developmental Disabilities Research Reviews. 4:20-25
Increasing research efforts and rapidly expanding knowledge in the neuroscientific foundations of learning, memory, and developmental disabilities have provided insights into the normal development and plasticity of neuronal circuits. Likewise, the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73a8564d071b478604f3ee505990c927
https://doi.org/10.1002/(sici)1098-2779(1998)4:1<20::aid-mrdd5>3.0.co
https://doi.org/10.1002/(sici)1098-2779(1998)4:1<20::aid-mrdd5>3.0.co
Autor:
Michael V. Johnston, Gregory J. Kato, James F. Casella, Steven N. Breiter, Alexander H. Hoon, Karen H Harum
Publikováno v:
Developmental medicine and child neurology. 41(11)
A 5-year old girl with cerebral palsy (CP), preterm birth, postnatal aortic thrombus, and cerebellar venous infarction who is homozygous for the thrombophilic factor-V Leiden (fVL) mutation is reported. The role of hereditary thrombophilic disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5617f58f31c03545f31353039c57ba3
https://pubmed.ncbi.nlm.nih.gov/10576642
https://pubmed.ncbi.nlm.nih.gov/10576642
Two unrelated patients with cryptic subtelomeric deletions of 22q13.3 were identified using FISH with the commercially available Oncor probe, D22S39. Proband 1 was found to have a derivative chromosome 22 resulting from the unbalanced segregation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a39755162192917cbee84a019d2c4c3
https://europepmc.org/articles/PMC1051025/
https://europepmc.org/articles/PMC1051025/
Publikováno v:
Pediatric Research. 43:124-124
Coffin-Lowry syndrome is an X-linked disorder characterized by facial dysmorphisms, cognitive impairment and skeletal anomalies. The phenotypic spectrum of CLS ranges from severe mental retardation to learning disabilities with severity of the skelet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75c903de44d9bac2d8d650b1efe13344
https://doi.org/10.1203/00006450-199804001-00737
https://doi.org/10.1203/00006450-199804001-00737
Publikováno v:
Developmental Medicine & Child Neurology; November 1999, Vol. 41 Issue: 11 p781-785, 5p