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Biomedical subjects

K R Meyers

Publications and source records attributed to K R Meyers.

9 recordsLinked to original sources
PubMed1996

Rey complex figure: memory error patterns and functional abilities.

The functional abilities of brain injured persons to live independently, were assessed using the Rancho Los Amigos Scale ratings of functional levels which were compared with memory error patterns on the Rey Complex Figure (Rey 1941) and the Recognition Trial developed by Meyers & Meyers (1995) Memory error patterns were described by Sohlberg & Mateer (1989), the least impaired memory error pattern was Retrieval, while Storage, Encoding and Attention patterns indicated greater defect Spearman rank order correlation revealed the strong association (r(S) = 86) of memory error pattern with Rancho Scale functional ratings In independent subjects 96 % achieved a Retrieval memory error pattern whereas 93% of subjects whose memory error pattern was poorer than a Retrieval pattern were unable to function independently Results indicate that patients obtaining a Retrieval (or better) memory error pattern may be expected to possess adequate cognitive resources for independent functioning.

Journal Article↗
PubMed1977

Mesothelial hyperplasia in hernia sacs.

Mesothelial hyperplasia is a benign condition, which simulates a neoplastic process. Since it may occur in hernia sacs this entity must be recognized by the urologist to prevent over-treatment.

Child, Preschool↗
PubMed1975

Myeloid, erythroid, and immune system defects in a family. A new stem-cell disorder?

Four of six siblings, offspring of Sicillian first cousins, developed a clinical disorder in early adulthood affecting the hematopoietic and immunoglobulin-producing systems. A female sibling died at age 21 with myeloid aplasia and agranulocytosis. A male sibling, at age 17, presented with erythroid and plasma cell aplasia with hypogammaglobulinemia. Two other female siblings, ages 21 and 35, had a lymphoproliferative disorder associated with hypogammaglobulinemia. In two of the affected subjects there was complete absence of the enzyme leukocyte alkaline phosphatase. Electron microscopic studies of the peripheral leukocytes from these two subjects and from one of the two asymptomatic siblings showed curious intranuclear and intracytoplasmic linear "crystalloid" structures in the mature neutrophils. It is postulated that the family contains a genetic defect, transmitted as an autosomal recessive by the heterozygous parents, that produces a stem-cell disorder manifested by myeloid, erythroid, and plasma cell aplasias, unique electron microscopic findings, and morphologic and functional abnormalities in later generations of cells.

Adolescent↗