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Abstract Pituitary tumors, that origin from excessive proliferation of a specific subtype of pituitary cell, are mostly benign tumors, but may cause significant morbidity in affected patients, including visual and neurologic manifestations from mass-effect, or endocrine syndromes caused by hormone hypersecretion

Treatment typically begins with weekly injections for several weeks, followed by monthly maintenance doses

Brenda Johnson, MATS, PA-C, explores the four primary forms of cobalamin

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(Shibata et al., 2016)), and with the depletion of intermediate cell specific transcripts in homozygous mutant cochleae (Fig