Kenton Holden to Muscle Hypotonia
This is a "connection" page, showing publications Kenton Holden has written about Muscle Hypotonia.
Connection Strength
0.980
-
Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies. J Child Neurol. 2015 Oct; 30(12):1664-8.
Score: 0.497
-
A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiency. Pediatr Res. 1997 Feb; 41(2):210-3.
Score: 0.141
-
Finding new etiologies of mental retardation and hypotonia: X marks the spot. Dev Med Child Neurol. 2008 Feb; 50(2):104-11.
Score: 0.075
-
Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant. J Child Neurol. 2008 Jan; 23(1):112-7.
Score: 0.075
-
Early onset alpha-mannosidosis with slow progression in three Hispanic males. Dev Med Child Neurol. 2007 Nov; 49(11):854-7.
Score: 0.074
-
Epidemiology of childhood Guillain-Barr? syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999. J Child Neurol. 2003 Nov; 18(11):741-7.
Score: 0.056
-
Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53.
Score: 0.024
-
X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7.
Score: 0.016
-
POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
Score: 0.015
-
X-linked myotubular myopathy: clinical observations in ten additional cases. Am J Med Genet. 1995 Nov 06; 59(2):168-73.
Score: 0.008