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  2. Charlotte Sumner - Wikipedia

    en.wikipedia.org/wiki/Charlotte_Sumner

    Charlotte Sumner Sumner in 2019, capturing images of brainstem sections from a patient who died of an inherited motoneuron disease. Alma mater Princeton University (B.A.) Perelman School of Medicine at the University of Pennsylvania (M.D.) Scientific career Fields Neurology, Neuroscience Institutions Johns Hopkins School of Medicine Charlotte Jane Sumner is an American neurologist. She is a ...

  3. Pain or Tingling in Your Feet? Podiatrists Share Top Shoes ...

    www.aol.com/pain-tingling-feet-podiatrists-share...

    The best shoes for neuropathy help manage pain to keep your feet comfortable. Here, podiatrists share their top picks, including Skechers, Hoka, and more.

  4. Peripheral neuropathy - Wikipedia

    en.wikipedia.org/wiki/Peripheral_neuropathy

    Peripheral neuropathy may be classified according to the number and distribution of nerves affected (mononeuropathy, mononeuritis multiplex, or polyneuropathy), the type of nerve fiber predominantly affected (motor, sensory, autonomic), or the process affecting the nerves; e.g., inflammation (), compression (compression neuropathy), chemotherapy (chemotherapy-induced peripheral neuropathy).

  5. Polyneuropathy - Wikipedia

    en.wikipedia.org/wiki/Polyneuropathy

    Additionally, BP control in those with diabetes is helpful, while intravenous immunoglobulin is used for multifocal motor neuropathy. [ 1 ] According to Lopate, et al., methylprednisolone is a viable treatment for chronic inflammatory demyelinative polyneuropathy (which can also be treated with intravenous immunoglobulin).

  6. Sensory neuronopathy - Wikipedia

    en.wikipedia.org/wiki/Sensory_neuronopathy

    Symptoms of sensory neuropathy may sometimes precede the cancer diagnosis by several months. Immune mediated sensory neuronopathy is commonly associated with Sjogrens syndrome. [5] Sjogren's is most commonly affected by a length dependent axonal sensorimotor neuropathy characterized by symptoms in the extremities.

  7. Spinocerebellar ataxia type 6 - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia_type_6

    Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Unlike other types, SCA 6 is not fatal.

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