Pages that link to "Q59554732"
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The following pages link to Michael Shy (Q59554732):
Displaying 50 items.
- Small nerve fiber involvement in CMT1A. (Q27312053) (← links)
- SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation (Q28240488) (← links)
- Peripheral neuropathy associated with eosinophilia-myalgia syndrome (Q28330752) (← links)
- Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells (Q28512857) (← links)
- Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2. (Q30009423) (← links)
- Structure and expression of proteolipid protein in the peripheral nervous system (Q30989179) (← links)
- Vitamin A controls epithelial/mesenchymal interactions through Ret expression (Q31804569) (← links)
- Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromes (Q33540227) (← links)
- Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A. (Q33567193) (← links)
- Introduction to the Third International Symposium on Charcot-Marie-Tooth disorders. (Q33787266) (← links)
- Regulation of myelin-specific gene expression. Relevance to CMT1. (Q33787310) (← links)
- Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease (Q33833588) (← links)
- Functional magnetic resonance imaging during urodynamic testing identifies brain structures initiating micturition (Q33836060) (← links)
- Functional Magnetic Resonance Imaging with Concurrent Urodynamic Testing Identifies Brain Structures Involved in Micturition Cycle in Patients with Multiple Sclerosis. (Q33873382) (← links)
- Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis. (Q34044153) (← links)
- Determinants of reduced health-related quality of life in pediatric inherited neuropathies (Q34098654) (← links)
- Distinct pathogenic processes between Fig4-deficient motor and sensory neurons. (Q34171101) (← links)
- Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease. (Q34174921) (← links)
- Demyelinating CMT--what's known, what's new and what's in store? (Q34459925) (← links)
- A molecular basis for hereditary motor and sensory neuropathy disorders. (Q34566358) (← links)
- Quality-of-life in Charcot-Marie-Tooth disease: the patient's perspective (Q34621607) (← links)
- Detection of copy number variation by SNP-allelotyping. (Q34624454) (← links)
- Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties. (Q34674307) (← links)
- Charcot-Marie-Tooth disease subtypes and genetic testing strategies (Q34681666) (← links)
- Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family (Q34733503) (← links)
- MFN2 mutations cause severe phenotypes in most patients with CMT2A. (Q34999364) (← links)
- Diagnosis and new treatments in genetic neuropathies. (Q35013208) (← links)
- Gain of glycosylation: a new pathomechanism of myelin protein zero mutations. (Q35859857) (← links)
- Reduced neurofilament expression in cutaneous nerve fibers of patients with CMT2E. (Q35892764) (← links)
- Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy (Q35984327) (← links)
- Myelin protein zero/P0 phosphorylation and function require an adaptor protein linking it to RACK1 and PKC alpha. (Q36118335) (← links)
- Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion (Q36132677) (← links)
- Charcot-Marie-Tooth disease: New insights from skin biopsy (Q36166978) (← links)
- Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy (Q36553011) (← links)
- Objective Evaluation of Overactive Bladder: Which Surveys Should I Use? (Q36630704) (← links)
- Inherited peripheral neuropathies. (Q36822088) (← links)
- X inactivation in females with X-linked Charcot-Marie-Tooth disease. (Q36852835) (← links)
- Prospective study of muscle cramps in Charcot-Marie-tooth disease. (Q36880895) (← links)
- Conduction block in PMP22 deficiency. (Q36912268) (← links)
- Update on Charcot-Marie-Tooth disease. (Q36937164) (← links)
- Neuropathy in a human without the PMP22 gene. (Q37013290) (← links)
- Lessons from London. (Q37039804) (← links)
- Phenotypic presentation of the Ser63Del MPZ mutation (Q37065127) (← links)
- Charcot-Marie-Tooth neuropathies: diagnosis and management. (Q37113862) (← links)
- Mitogen-expanded Schwann cells retain the capacity to myelinate regenerating axons after transplantation into rat sciatic nerve (Q37210728) (← links)
- Inherited neuropathies: clinical overview and update. (Q37571617) (← links)
- Effect of pain in pediatric inherited neuropathies (Q37623195) (← links)
- Biology of peripheral inherited neuropathies: Schwann cell axonal interactions. (Q37708112) (← links)
- Axonal Charcot-Marie-Tooth disease. (Q37926443) (← links)
- Charcot-Marie-Tooth disease and related genetic neuropathies. (Q38027305) (← links)