Piagetian scales and the Bender visual motor gestalt test (BT) were applied to 28 subjects with universal 45, X Turner syndrome (TS), and their respective controls, in order to investigate their cognitive performance. Dermatoglyphics were also analyzed to obtain clues concerning embryological changes that may have appeared during development of the nervous system and could be associated with cognitive performance of TS patients. Dermatoglyphic pattern distribution was similar to that reported in previous studies of TS individuals: ulnar loops in the digital patterns and finger ridge, a-b, and A'-d counts were more frequent, while arch and whorl patterns were less frequent compared to controls. However, we did not find higher frequencies of ...
Analysis of brain structure in Turner syndrome (TS) provides the opportunity to identify the consequ...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
Turner's syndrome is a sporadic disorder of human females in which all or part of one X chromosome i...
Piagetian scales and the Bender visual motor gestalt test (BT) were applied to 28 subjects with univ...
We reviewed the literature on Turner Syndrome (TS) from 1962 until March 2003 with respect to the fo...
Item does not contain fulltextWe reviewed the literature on Turner Syndrome (TS) from 1962 until Mar...
A síndrome de Turner (ST) é uma aneuploidia com incidência populacional estimada de 1:2.500-3.000 da...
Turner Syndrome (TS) is a genetic condition characterized by the partial or complete loss of one se...
Purpose Patients with Turner syndrome (TS) have distinct neurocognitive and psychosocial characteris...
Girls and women with Turner syndrome (TS) have a completely or partially missing X chromosome. Exten...
X-monosomy is a form of Turner syndrome (TS) in which an entire X chromosome is missing. It is usual...
Compared short-term verbal memory, sustained attention, and impulsivity in 13 children with Turner s...
Turner syndrome (TS) is associated with a characteristic neurocognitive profile that includes impair...
Abstract Background Turner syndrome is the result of the partial or complete absence of an X chromos...
International audienceAnalysis of brain structure in Turner syndrome (TS) provides the opportunity t...
Analysis of brain structure in Turner syndrome (TS) provides the opportunity to identify the consequ...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
Turner's syndrome is a sporadic disorder of human females in which all or part of one X chromosome i...
Piagetian scales and the Bender visual motor gestalt test (BT) were applied to 28 subjects with univ...
We reviewed the literature on Turner Syndrome (TS) from 1962 until March 2003 with respect to the fo...
Item does not contain fulltextWe reviewed the literature on Turner Syndrome (TS) from 1962 until Mar...
A síndrome de Turner (ST) é uma aneuploidia com incidência populacional estimada de 1:2.500-3.000 da...
Turner Syndrome (TS) is a genetic condition characterized by the partial or complete loss of one se...
Purpose Patients with Turner syndrome (TS) have distinct neurocognitive and psychosocial characteris...
Girls and women with Turner syndrome (TS) have a completely or partially missing X chromosome. Exten...
X-monosomy is a form of Turner syndrome (TS) in which an entire X chromosome is missing. It is usual...
Compared short-term verbal memory, sustained attention, and impulsivity in 13 children with Turner s...
Turner syndrome (TS) is associated with a characteristic neurocognitive profile that includes impair...
Abstract Background Turner syndrome is the result of the partial or complete absence of an X chromos...
International audienceAnalysis of brain structure in Turner syndrome (TS) provides the opportunity t...
Analysis of brain structure in Turner syndrome (TS) provides the opportunity to identify the consequ...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
Turner's syndrome is a sporadic disorder of human females in which all or part of one X chromosome i...