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STEFAN TORELLI, MD
MD
Internal Medicine Physician
NPI: 1942887419Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A183218(CA)
Research & Publications (20)
Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy.
PMID 17044012·Ann Neurol·2006
5-case
Histopathological evaluation of treatment with chondroitin sulphate for osteoarthritis induced by continuous immobilization in rabbits.
PMID 15703011·J Vet Med A Physiol Pathol Clin Med·2005
7-preclinical
Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2I.
PMID 16288869·Neuromuscul Disord·2005
4-observational
Tuning the decay time of lanthanide-based near infrared luminescence from micro- to milliseconds through d-->f energy transfer in discrete heterobimetallic complexes.
PMID 15779094·Chemistry·2005
8-other
Ruthenium(II) as a novel "labile" partner in thermodynamic self-assembly of heterobimetallic d-f triple-stranded helicates.
PMID 15252796·Chemistry·2004
8-other
Radiography, computed tomography and magnetic resonance imaging at 0.5 Tesla of mechanically induced osteoarthritis in rabbit knees.
PMID 15064812·Braz J Med Biol Res·2004
4-observational
[Incidence and primary prevention of complications related to the placement of dental implants].
PMID 11508118·Rev Belge Med Dent (1984)·2001
6-review
A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity.
PMID 18691338·Brain Pathol·2009
4-observational
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant.
PMID 18195152·Arch Neurol·2008
5-case
Spectroscopic and computational studies of (mu-oxo)(mu-1,2-peroxo)diiron(III) complexes of relevance to nonheme diiron oxygenase intermediates.
PMID 18811130·J Phys Chem A·2008
8-other
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan.
PMID 17878207·Brain·2007
4-observational
Muscular dystrophies due to defective glycosylation of dystroglycan.
PMID 18646561·Acta Myol·2007
6-review
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human.
PMID 17826093·Neuromuscul Disord·2007
8-other
Design of iron chelators: syntheses and iron (III) complexing abilities of tripodal tris-bidentate ligands.
PMID 16841245·Biometals·2006
6-review
Multifrequency EPR and redox reactivity investigations of a bis(mu-thiolato)-dicopper(II,II) complex.
PMID 17140245·Inorg Chem·2006
8-other
Structural, thermodynamic, and mesomorphic consequences of replacing nitrates with trifluoroacetate counteranions in ternary lanthanide complexes with hexacatenar tridentate ligands.
PMID 16562955·Inorg Chem·2006
8-other
Mutated fukutin-related protein (FKRP) localises as wild type in differentiated muscle cells.
PMID 16055117·Exp Cell Res·2005
7-preclinical
Syncoilin upregulation in muscle of patients with neuromuscular disease.
PMID 16124004·Muscle Nerve·2005
4-observational
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy.
PMID 15661757·Hum Mol Genet·2005
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 300 PASTEUR DR, ALWAY BUILD M211, MC 5187
STANFORD, CA 94305 - Phone
- (650) 723-6661
Quick Facts
- NPI
- 1942887419
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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