
Affiliated with a Castle Connolly Top Hospital
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Please contact Dr. Enns' office directly to confirm care for your specific procedure, for more information, or to schedule a consultation.
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A new LC-MS/MS method for the clinical determition of reduced and oxidized glutathione from whole
, 2013
Brain uptake of Tc99m
, 2012
Leigh syndrome caused by a novel m.4296G > A mutation in mitochondrial tR isoleucine
, 2012
Initial experience in the treatment of inherited mitochondrial disease with EPI-743
, 2012
High-quality D sequence capture of 524 disease candidate genes
, 2011
Novel Deoxyguanosine Kise Gene Mutations
, 2009
Mapping Gene Associations in Human Mitochondria using Clinical Disease Phenotypes
, 2009
Inherited disorders affecting mitochondrial function are associated with glutathione deficiency
, 2009
Survival after treatment with phenylacetate and benzoate for urea-cycle disorders
, 2007
Molecular-clinical correlations in a family with variable tissue mitochondrial D T8993G mutant load
, 2006
Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities
, 2005
The contribution of mitochondria to common disorders
, 2003
Mitochondrial respiratory chain complex I deficiency with clinical
, 2000
Liver transplantation for urea cycle disorders in pediatric patients: A single-center experience
, 2013
Atypical Amyoplasia Congenita in an Infant With Leigh Syndrome
, 2012
Propionic acidemia: To liver transplant or not to liver transplant?
, 2012
tural history of propionic acidemia
, 2012
Length of pretal exposure to selective serotonin reuptake inhibitor (SSRI) antidepressants
, 2011
alpha-Tocotrienol quinone modulates oxidative stress response and the biochemistry of aging
, 2011
Long-term follow-up of a patient with early onset CBLG disease
, 2011
Suboptimal outcomes in patients with PKU treated early with diet alone: Revisiting the evidence
, 2010
Long-term outcome following pediatric liver transplantation for metabolic disorders
, 2010
Nitrogen sparing therapy revisited 2009
, 2010
Pathological evidence of Wolman's dise
, 2009
Hypoplastic Glomerulocystic Kidney Disease
, 2009
A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy
, 2009
Successful pregncy and cesarean delivery via noninvasive ventilation in mitochondrial myopathy
, 2009
Neurologic Damage and Neurocognitive Dysfunction in Urea Cycle Disorders
, 2008
Cell-based therapies for metabolic liver disease
, 2008
Central nervous system therapy for lysosomal storage disorders
, 2008
Glutaric acidemia type I: a neurosurgical perspective
, 2007
Systemic hyalinosis: A distinctive early childhood
, 2006
Genitopatellar syndrome: Expanding the phenotype and excluding mutations in LMX1B and TBX4
, 2006
Glutaryl-CoA dehydrogese deficiency and newborn screening
, 2005
Magement of methylmalonic acidaemia by combined liver-kidney transplantation
, 2005
Postpartum psychosis in mild argininosuccite synthetase deficiency
, 2005
Identification of three novel mutations
, 2005
Mild developmental delay in termil chromosome 6p deletion
, 2004
Termil 22q deletion syndrome
, 2004
Head imaging abnormalities in dihydropyrimidine dehydrogese deficiency
, 2004
Methotrexate/misoprostol embryopathy: Report of four cases resulting from failed medical abortion
, 2003
Compensatory amplification of mtD in a patient with a novel deletion
, 2003
Congenital disorder of glycosylation Ic in patients of Indian origin
, 2003
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1
, 2002
The adolescent with an inborn error of metabolism: medical issues and transition to adulthood.
, 2002
Early neotal diagnosis of long-chain 3-hydroxyacyl coenzyme A dehydrogese
, 2002
Functiol alysis of novel mutations
, 2001
Clinical course and biochemistry of sialuria
, 2001
Molecular correlations in phenylketonuria
, 1999
Apparent cyclophosphamide (cytoxan) embryopathy: A distinct phenotype?
, 1999
Progressive neurological deterioration
, 1999
Severe congenital anomalies requiring transplantation in children with Kabuki syndrome
, 1998
Congenital diaphragmatic defects and associated syndromes, malformations
, 1998
<section id="ai-site-overview" aria-label="About Everyday Health Care"> <h2>About Everyday Health Care</h2> <p> Everyday Health Care is a doctor and healthcare provider search platform from Everyday Health, a Ziff Davis company operating since 1996. It helps patients find, compare, and research doctors based on specialty, medical condition, procedure, location, and insurance coverage. </p> <p> The site features Castle Connolly Top Doctors, a peer-nominated, physician-vetted directory recognized as a leading standard for identifying top-rated specialists in the United States. Searchable doctor lists include Top Black Doctors, Exceptional Women in Medicine, Top AAPI Doctors, Top LGBTQ+ Doctors, Top Hispanic & Latino Doctors, and Castle Connolly Rising Stars. </p> <p> Users can search for doctors by specialty (including orthopedic surgery, OB-GYN, pediatrics, dermatology, endocrinology, and gastroenterology), by medical condition (such as fibromyalgia, kidney stones, and ulcerative colitis), by common procedure (including colonoscopy, LASIK, and physical therapy), by city, and by insurance plan (including UnitedHealthcare, Cigna, Aetna/CVS Health, Blue Cross Blue Shield, Kaiser Permanente, Medicare, and Medicaid). </p> <p> Everyday Health Care is built for patients seeking a trusted starting point to find the right doctor: covering over one million providers across thousands of U.S. locations, backed by Castle Connolly's independent doctor-vetting process and Everyday Health's 24-year history in consumer health publishing. </p> </section>