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UnknownThe value of Eye Movement Desensitization Reprocessing in the treatment of tinnitus: study protocol for a randomized controlled trial.
Not available
S-EPMC6327461 | biostudies-literature
UnknownA new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene.
Not available
S-EPMC1559536 | biostudies-literature
UnknownBimodal Therapy for Chronic Subjective Tinnitus: A Randomized Controlled Trial of EMDR and TRT Versus CBT and TRT.
Not available
S-EPMC7511540 | biostudies-literature
UnknownA second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36.
Not available
S-EPMC1235283 | biostudies-literature
UnknownNonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
Not available
S-EPMC1181955 | biostudies-literature
UnknownAssociation of bone morphogenetic proteins with otosclerosis.
Not available
S-EPMC2669162 | biostudies-literature
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