Page last updated: 2024-08-17

lysine and Deafness, Transitory

lysine has been researched along with Deafness, Transitory in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wolf, B1
Bau, AE; de Zwart-Storm, EA; Foelster-Holst, R; Frank, J; Graziadio, C; Kamps, MA; Martin, PE; Paskulin, GA; Rosa, RF; van Geel, M; van Steensel, MA; Zen, PR1
Gao, W; Guo, X; Hao, J; Hu, R; Kunishima, S1
Aoki, C; Fujisawa, S; Karthikeyan, O; Kotak, VC; Lee, FA; Sanes, DH1
Hoppe, B; Stefanelli, M; Woolridge, D1

Reviews

1 review(s) available for lysine and Deafness, Transitory

ArticleYear
Clinical issues and frequent questions about biotinidase deficiency.
    Molecular genetics and metabolism, 2010, Volume: 100, Issue:1

    Topics: Animals; Biotin; Biotinidase Deficiency; Evidence-Based Medicine; False Positive Reactions; Hearing Loss; Humans; Infant, Newborn; Infant, Premature; Lysine; Neonatal Screening; Protein Binding; Specimen Handling

2010

Other Studies

4 other study(ies) available for lysine and Deafness, Transitory

ArticleYear
Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes.
    Experimental dermatology, 2011, Volume: 20, Issue:5

    Topics: Adult; Asparagine; Aspartic Acid; Cell Membrane; Child; Connexin 26; Connexins; Cytoplasm; Endoplasmic Reticulum; Female; Fluoresceins; Gap Junctions; Hearing Loss; HeLa Cells; Humans; Hypertrichosis; Keratoderma, Palmoplantar; Keratosis; Lysine; Male; Mutation, Missense; Nails, Malformed; Protein Transport; Skin; Skin Diseases; Syndrome; Transfection; Tyrosine

2011
A large family with MYH9 disorder caused by E1841K mutation suffering from serious kidney and hearing impairment and cataracts.
    Annals of hematology, 2012, Volume: 91, Issue:7

    Topics: Amino Acid Substitution; Cataract; Family Characteristics; Glutamic Acid; Hearing Loss; Humans; Kidney Diseases; Lysine; Male; Middle Aged; Molecular Motor Proteins; Mutation, Missense; Myosin Heavy Chains; Pedigree; Severity of Illness Index

2012
Hearing loss raises excitability in the auditory cortex.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005, Apr-13, Volume: 25, Issue:15

    Topics: Adaptation, Physiological; Animals; Animals, Newborn; Auditory Cortex; Cell Count; Cochlear Nucleus; Disease Models, Animal; Dose-Response Relationship, Radiation; Drug Interactions; Electric Stimulation; Excitatory Amino Acid Antagonists; Gerbillinae; Hearing Loss; Immunohistochemistry; In Vitro Techniques; Lysine; Microscopy, Immunoelectron; Neural Inhibition; Neuronal Plasticity; Neurons; Patch-Clamp Techniques; Receptors, N-Methyl-D-Aspartate; Synapses; Synaptic Transmission

2005
Susac syndrome with frontal intermittent rhythmic delta activity (FIRDA).
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2006, Volume: 33, Issue:4

    Topics: Adult; Brain Diseases; Calcium Channel Blockers; Delta Rhythm; Gait Disorders, Neurologic; Hearing Loss; Humans; Lysine; Magnetic Resonance Imaging; Male; Methylprednisolone; Neuroprotective Agents; Nimodipine; Retinal Artery Occlusion; Vision Disorders

2006