Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973
The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973
Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972
Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972
Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972
Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972
Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972
Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971
Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971
"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971
Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971
Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971
Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970
Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970
Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969
Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969
Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969
The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969
Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969
Biochemical Abnormalities of the Sarcoplasmic Reticulum in Muscular Dystrophy
NEJM 290:184, Samaha,F.,et al, 1969
Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968
Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968
The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968
Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967
The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967
Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967
Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967
Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967
Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966
The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965
Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963
Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850
Teaching NeuroImage: The House Soign in Behavioral Varianht Frontotemporal Dementia
Neurol 104:e213519, Ioannidis,S.,et al, 2025
A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025
"Innumerable" lesion burden on brain MRI - a diagnostic approach
Diagnosis doi.org/10.1515/dx- 2025-2029, Finelli,P.F., 2025
A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024
Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024
A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024
Repurposing Erectile Dysfunction Medication for Alzheimer Disease Prevention
Neurol 102:e209180, Yasara,S., & Nidadavolu,L., 2024
An Unusual Etiology of Lumbosacral Plexopathy in a Patient with HIV
Neurol 103:e209930, Madduluri,B.,et al, 2024
A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024
A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024
Sulcal Hyperintensity as an Early Imaging Finding in Cerebral Amyloid Angiopathy-Related Inflammation
Neurol 103:e210084, Panteleienko,L.,et al, 2024
Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
Neurol 103:e209586, Taborda,M.H.,et al, 2024
Diagnosing Cerebral Amyloid Angiopathy-Related Inflammation
Neurol 103:e209548, Charidimou,A., 2024
Occult Amyloid-B-Related Angiitis:Neuroimaging Findings at 1.5T, 3T, and 7T MRI
AJNR 45:1013-1018, Ozutemlz,C.,et al, 2024
Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023
A Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,J.,et al, 2023
Clinical,Neuroimaging,and Genetic Markers in Cerebral Amyloid Angiopatny-Related Inflammation:A Systematic Review and Meta-Analusis
Stroke 54:178-188, Theodorou,A.,et al, 2023
Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023