|1.||Hamner, Heather C: 3 articles (04/2014 - 05/2013)|
|2.||Tinker, Sarah C: 3 articles (04/2014 - 05/2013)|
|3.||Dowling, Nicole F: 2 articles (10/2013 - 05/2013)|
|4.||Rodríguez-Sánchez, Felicidad: 1 article (11/2015)|
|5.||Gutiérrez, Gema: 1 article (11/2015)|
|6.||Mora-López, Francisco: 1 article (11/2015)|
|7.||Marín, Rosario: 1 article (11/2015)|
|8.||Arroyo, Diego: 1 article (11/2015)|
|9.||Ley-Martos, Miriam: 1 article (11/2015)|
|10.||Zhu, Yijian: 1 article (12/2014)|
|1.||Mental Retardation (Idiocy)
04/15/1992 - "Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28."
01/01/1974 - "The MASA syndrome: a new heritable mental retardation syndrome."
04/01/1994 - "The MASA syndrome is an X-linked disorder with mental retardation, spastic paraparesis, and adducted thumbs as the most characteristic features. "
01/01/1994 - "X-linked hydrocephalus and the X-linked MASA syndrome (Mental retardation. "
06/01/1996 - "These findings were consistent with the MASA spectrum (mental retardation-aphasia-shuffling gait-adducted thumbs) present in the older brother. "
06/01/1996 - "Transvaginal sonographic detection of adducted thumbs, hydrocephalus, and agenesis of the corpus callosum at 22 postmenstrual weeks: the masa spectrum or L1 spectrum. "
03/22/1996 - "These results provide, for the first time, direct demonstration of the deleterious effects of hydrocephalus/MASA mutations on two intrinsic properties of L1."
03/22/1996 - "Differential effects of two hydrocephalus/MASA syndrome-related mutations on the homophilic binding and neuritogenic activities of the cell adhesion molecule L1."
12/01/2000 - "The recent identification of a common etiology among MASA syndrome (McKusick 303300), X-linked hydrocephalus (HSAS) (McKusick 307000) and other related neurological disorders, which had previously been considered distinct nosological entities, allowed us to diagnose MASA syndrome in a male fetus in a primigravida at the 29th week of gestation by sonographic signs of the MASA spectrum such as hydrocephalus and hypoplasia of corpus callosum. "
07/01/1994 - "L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus."
|3.||Hereditary Spastic Paraplegia
|5.||Anxiety Disorders (Anxiety Disorder)
|1.||Adducted Thumbs) Syndrome Shuffling Gait Aphasia MASA (Mental Retardation
|3.||Steroid 21-Hydroxylase (21 Hydroxylase)
|4.||Proteins (Proteins, Gene)
|5.||Neural Cell Adhesion Molecule L1 (L1 Cell Adhesion Molecule)
|6.||DNA (Deoxyribonucleic Acid)
|7.||Folic Acid (Vitamin M)
|9.||Immunoglobulin G (IgG)
|10.||Immunoglobulin A (IgA)