Back to Search
LEO KRATZ, DO
DO
Family Medicine Physician
NPI: 1326077322Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
OS007275E(PA)H0046721(PA)
Research & Publications (18)
Dehydrosteroid measurements in maternal urine or serum for the prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS).
PMID 17702049·Am J Med Genet A·2007
3-trial
Identifying Smith-Lemli-Opitz syndrome in conjunction with prenatal screening for Down syndrome.
PMID 16832833·Prenat Diagn·2006
4-observational
Abnormalities of cholesterol metabolism in autism spectrum disorders.
PMID 16874769·Am J Med Genet B Neuropsychiatr Genet·2006
8-other
Noninvasive assessment of brain injury in a canine model of hypothermic circulatory arrest using magnetic resonance spectroscopy.
PMID 16631640·Ann Thorac Surg·2006
7-preclinical
Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy.
PMID 16446309·Hum Mol Genet·2006
7-preclinical
Valproic acid prevents brain injury in a canine model of hypothermic circulatory arrest: a promising new approach to neuroprotection during cardiac surgery.
PMID 16731160·Ann Thorac Surg·2006
4-observational
Pharmacokinetics and safety of the MRI contrast agent gadoversetamide injection (OptiMARK) in healthy pediatric subjects.
PMID 15167099·Invest Radiol·2004
8-other
Response of obligate heterozygotes for phytosterolemia to a low-fat diet and to a plant sterol ester dietary challenge.
PMID 12671028·J Lipid Res·2003
3-trial
Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiency.
PMID 12812989·Hum Mol Genet·2003
5-case
Abnormal sterol metabolism in a patient with Antley-Bixler syndrome and ambiguous genitalia.
PMID 12116245·Am J Med Genet·2002
5-case
Desmosterolosis presenting with multiple congenital anomalies and profound developmental delay.
PMID 12457401·Am J Med Genet·2002
5-case
Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith--Lemli--Opitz syndrome.
PMID 11230174·Hum Mol Genet·2001
7-preclinical
Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndrome.
PMID 11260610·Prenat Diagn·2001
8-other
Lethal form of chondrodysplasia punctata with normal plasmalogen and cholesterol biosynthesis.
PMID 11169563·Am J Med Genet·2001
5-case
CHILD syndrome caused by deficiency of 3beta-hydroxysteroid-delta8, delta7-isomerase.
PMID 10710233·Am J Med Genet·2000
5-case
Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome.
PMID 11186897·Am J Med Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 6 locations total
- Address
- 3106 PHILADELPHIA AVE
CHAMBERSBURG, PA 17201 - Phone
- (717) 264-3644
Locations (6)
Practice Location
3106 PHILADELPHIA AVE, CHAMBERSBURG, PA
(717) 264-3644
Practice Location
8131 SPYGLASS HILL DR, FAYETTEVILLE, PA
(717) 749-3181
Practice Location
24 ANTRIM COMMONS DR, GREENCASTLE, PA
(717) 597-5553
Practice Location
2 KEEFER DR, MERCERSBURG, PA
(717) 328-2119
Practice Location
46 WALNUT BOTTOM RD STE 200, SHIPPENSBURG, PA
(717) 532-4148
Practice Location
601 E MAIN ST, WAYNESBORO, PA
(717) 765-5085
Quick Facts
- NPI
- 1326077322
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 6
- Publications
- 18
Are you this provider?
Claim Your Profile