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RENEE SCOLA, MD

MD

Internal Medicine Physician

NPI: 1457344970Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

036100929(IL)

Research & Publications (20)

Toxic myopathies: muscle biopsy features.
PMID 17420833·Arq Neuropsiquiatr·2007
8-other
A novel missense mutation pattern of the GCH1 gene in dopa-responsive dystonia.
PMID 18345435·Arq Neuropsiquiatr·2007
5-case
[Spheroid body myopathy: case report].
PMID 16100986·Arq Neuropsiquiatr·2005
5-case
Simvastatin-induced mononeuropathy multiplex: case report.
PMID 15273860·Arq Neuropsiquiatr·2004
5-case
[Peripheral neuropathy and myositis in idiopathic hypereosinophilic syndrome: case report].
PMID 15122451·Arq Neuropsiquiatr·2004
5-case
Myotonia congenita and myoadenylate deaminase deficiency: case report.
PMID 12806508·Arq Neuropsiquiatr·2003
5-case
Ankylosing spondylitis and central core disease: case report.
PMID 14513182·Arq Neuropsiquiatr·2003
5-case
[Distal myasthenia gravis: case report].
PMID 12715034·Arq Neuropsiquiatr·2003
5-case
Amyloidotic muscle pseudohypertrophy: case report.
PMID 11588639·Arq Neuropsiquiatr·2001
5-case
Inflammatory myopathy on HTLV-I infection: case report.
PMID 11299445·Arq Neuropsiquiatr·2001
5-case
Symptomatic muscle involvement in neurosarcoidosis: a clinicopathological study of 5 cases.
PMID 11460177·Arq Neuropsiquiatr·2001
8-other
Diagnosis of dermatomyositis and polymyositis: a study of 102 cases.
PMID 11018813·Arq Neuropsiquiatr·2000
4-observational
Acquired slow-channel syndrome.
PMID 11003795·Muscle Nerve·2000
5-case
Electrophysiological study in synaptic congenital myasthenic syndrome: end-plate acetylcholinesterase deficiency.
PMID 19623452·Arq Neuropsiquiatr·2009
5-case
Spinal cord arteriovenous malformation: a pediatric presentation.
PMID 19623460·Arq Neuropsiquiatr·2009
5-case
Neurofibromatosis 1 associated with spinal muscular atrophy.
PMID 19135626·Pediatr Neurol·2009
5-case
A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia.
PMID 19307729·J Clin Invest·2009
8-other
Botulinum toxin type A in the treatment of lower-limb spasticity in children with cerebral palsy.
PMID 19330214·Arq Neuropsiquiatr·2009
3-trial
NMO-IgG positive neuromyelitis optica in a patient with myasthenia gravis but no thymectomy.
PMID 18703206·J Neurol Sci·2008
5-case
Swallowing dysfunction in hereditary neuropathy with liability to pressure palsies.
PMID 19099137·Arq Neuropsiquiatr·2008
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
676 N SAINT CLAIR ST, SUITE 2300
CHICAGO, IL 60611

Location

Practice Location

676 N SAINT CLAIR ST, CHICAGO, IL
(312) 926-6000

Quick Facts

NPI
1457344970
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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