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Annals of the New York Academy of Sciences, ISSN 0077-8923, 11/2015, Volume 1356, Issue 1, pp. 45 - 79
Ca2+ release‐activated Ca2+ (CRAC) channels mediate a specific form of Ca2+ influx called store‐operated Ca2+ entry (SOCE) that contributes to the function of... 
calcium | disease | thrombocytopenia | channelopathy | enamel | CRAC channel | ameloblast | platelets | York platelet syndrome | mutation | STIM1 | muscular hypotonia | autoimmunity | Ca2 | Stormorken syndrome | SOCE | ORAI1 | skeletal muscle | tubular aggregate myopathy | Autoimmunity | Thrombocytopenia | Calcium | Disease | Channelopathy | Tubular aggregate myopathy | Enamel | Muscular hypotonia | Skeletal muscle | Mutation | Platelets | Ameloblast | OPERATED CA2+ ENTRY | SEVERE COMBINED IMMUNODEFICIENCY | IMMUNOLOGY | ACTIVATED CALCIUM-CHANNEL | CLASSIC KAPOSI-SARCOMA | DENTAL ENAMEL CELLS | INHERITED THROMBOCYTOPENIC DISORDER | T-CELL DEVELOPMENT | ELECTRON-DENSE CHAINS | STROMAL INTERACTION MOLECULE-1 | Stromal Interaction Molecule 1 | Muscle Hypotonia - genetics | Membrane Proteins - genetics | Humans | Autoimmune Diseases - immunology | Channelopathies - immunology | Neoplasm Proteins - immunology | Membrane Proteins - immunology | Severe Combined Immunodeficiency - immunology | Channelopathies - pathology | ORAI1 Protein | Autoimmune Diseases - genetics | Muscle Hypotonia - pathology | Severe Combined Immunodeficiency - genetics | Channelopathies - genetics | Calcium Channels - immunology | Severe Combined Immunodeficiency - pathology | Muscle Hypotonia - immunology | Neoplasm Proteins - genetics | Calcium Channels - genetics | Human | Proteins | Mutations | Teeth | Patients | Channels | Diseases | Defects
Journal Article
2011, Rehabilitation therapy in video
This video highlights the development of a child who has a primary diagnosis of congenital hypotonia of unknown etiology. Footage is provided from age 8 years... 
Muscle hypotonia in children
Web Resource
2011, Rehabilitation therapy in video
This video highlights the development of a child who has a primary diagnosis of congenital hypotonia of unknown etiology. Footage is provided from age 31... 
Muscle hypotonia in children
Web Resource
Journal Article
Nature Communications, ISSN 2041-1723, 2016, Volume 7, Issue 1, p. 11491
Journal Article
Clinical Infectious Diseases, ISSN 1058-4838, 09/2016, Volume 63, Issue 6, pp. 737 - 745
Journal Article
Journal Article
Journal of developmental and behavioral pediatrics : JDBP, ISSN 0196-206X, 09/2017, Volume 38, Issue 7, pp. 556 - 557
CASE: David is a 22-month-old boy who is new to your practice. He recently moved from a rural area in the Midwest. His father is in the United States Air... 
feeding difficulty | congenital hypotonia | BEHAVIORAL SCIENCES | PEDIATRICS | sensory processing disorder | PSYCHOLOGY, DEVELOPMENTAL | Muscle Hypotonia - complications | Developmental Disabilities - etiology | Humans | Infant | Male | Developmental Disabilities - diagnosis | Muscle Hypotonia - congenital | Muscle Hypotonia - diagnosis
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2016, Volume 98, Issue 4, pp. 782 - 788
Journal Article
Clinics in Perinatology, ISSN 0095-5108, 06/2015, Volume 42, Issue 2, pp. 363 - 371
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 07/2011, Volume 53, Issue 7, pp. 586 - 599
Aim  Hypotonia is a symptom of diminished tone of skeletal muscle associated with decreased resistance of muscles to passive stretching, which can be caused by... 
PEDIATRICS | CLINICAL NEUROLOGY | Pediatrics - trends | Muscle Hypotonia - genetics | Muscle Hypotonia - physiopathology | Prognosis | Humans | Child | Muscle Hypotonia - classification | Muscle Hypotonia - diagnosis
Journal Article