-
1
-
-
0000345901
-
Some polyneuropathies (PNs) in insulin-requiring adult-onset diabetes (IRAOD) can benefit remarkably from anti-dysimmune treatments
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Engel WK, Prentice AF. (1993) Some polyneuropathies (PNs) in insulin-requiring adult-onset diabetes (IRAOD) can benefit remarkably from anti-dysimmune treatments. Neurology 43, 255-256.
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(1993)
Neurology
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-
Engel, W.K.1
Prentice, A.F.2
-
2
-
-
25344468855
-
In type-2 diabetes, diabetic neuropathy is usually responsive to intravenous IgG (IVIG) treatment, ergo presumably dysimmune
-
Engel, WK. (2002) In type-2 diabetes, diabetic neuropathy is usually responsive to intravenous IgG (IVIG) treatment, ergo presumably dysimmune. Acta Myologica 21, A79.
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(2002)
Acta Myologica
, vol.21
-
-
Engel, W.K.1
-
3
-
-
1542433326
-
Intravenous immunoglobulin (IVIG) - an often-overlooked treatment - produces rapid, remarkable, sustained benefit in "diabetic neuropathy complex", suggesting a dysimmune mechanism
-
Engel WK. (1997) Intravenous immunoglobulin (IVIG) - an often-overlooked treatment - produces rapid, remarkable, sustained benefit in "diabetic neuropathy complex", suggesting a dysimmune mechanism. Ann Neurol 42, 414.
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(1997)
Ann Neurol
, vol.42
, pp. 414
-
-
Engel, W.K.1
-
4
-
-
1542720562
-
Intravenous immunoglobulin G is remarkably beneficial in chronic immune dysschwannian/ dysneuronal polyneuropathy, diabetes-2 neuropathy, and potentially in severe acute respiratory syndrome
-
Engel WK. (2003) Intravenous immunoglobulin G is remarkably beneficial in chronic immune dysschwannian/ dysneuronal polyneuropathy, diabetes-2 neuropathy, and potentially in severe acute respiratory syndrome. Acta Myologica 22, 97-103.
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(2003)
Acta Myologica
, vol.22
, pp. 97-103
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-
Engel, W.K.1
-
5
-
-
84885548507
-
"Pseudo-lupus", benign neutropenia, and other probable non-worrisome blood-component changes due to IVIG treatment
-
Engel WK. (2006) "Pseudo-lupus", benign neutropenia, and other probable non-worrisome blood-component changes due to IVIG treatment. Neuromuscul Disord 16, 647-648.
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(2006)
Neuromuscul Disord
, vol.16
, pp. 647-648
-
-
Engel, W.K.1
-
6
-
-
84885489520
-
Longer-term (>3 months), IVIG treatment to optimize clinical benefit and cellular protection usually requires an individualized adjustable schedule - not fixed regimentation
-
Engel WK. (2006) Longer-term (>3 months), IVIG treatment to optimize clinical benefit and cellular protection usually requires an individualized adjustable schedule - not fixed regimentation. Neuromuscul Disord 16, 703-704.
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(2006)
Neuromuscul Disord
, vol.16
, pp. 703-704
-
-
Engel, W.K.1
-
7
-
-
70349671018
-
Intravenous immunoglobulin in relapsing-remittin multiple sclerosis: a dose-finding trial
-
Engel WK. (2009) Intravenous immunoglobulin in relapsing-remittin multiple sclerosis: a dose-finding trial. Neurology 73, 1077-1078.
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(2009)
Neurology
, vol.73
, pp. 1077-1078
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-
Engel, W.K.1
-
8
-
-
79953825265
-
Multi-microcramps (MMC) syndrome: a new pathogenic concept of subtle lower motor-neuron (LMN) lability causing very disturbing, continuing muscle pains, sometimes gratifying treatable - but often misinterpreted as mysterious "fibromyalgia" or "psychogenic"
-
Engel WK. (2010) Multi-microcramps (MMC) syndrome: a new pathogenic concept of subtle lower motor-neuron (LMN) lability causing very disturbing, continuing muscle pains, sometimes gratifying treatable - but often misinterpreted as mysterious "fibromyalgia" or "psychogenic". Neurology 74, A465.
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Neurology
, vol.74
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-
Engel, W.K.1
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9
-
-
79953830103
-
Symptomatic treatment for muscle cramps (an evidence-based review)
-
Mahajan S, Engel WK. (2010) Symptomatic treatment for muscle cramps (an evidence-based review). Letter to the Editor. Neurology 75, 1397-1398.
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(2010)
Letter to the Editor. Neurology
, vol.75
, pp. 1397-1398
-
-
Mahajan, S.1
Engel, W.K.2
-
10
-
-
0015226910
-
Myasthenia gravis: a new hypothesis of the pathogenesis and a new form of treatment
-
Engel WK, Warmolts JR. (1971) Myasthenia gravis: a new hypothesis of the pathogenesis and a new form of treatment. Ann N Y Acad Sci 183, 72-87.
-
(1971)
Ann N Y Acad Sci
, vol.183
, pp. 72-87
-
-
Engel, W.K.1
Warmolts, J.R.2
-
11
-
-
0015495496
-
Benefit from alternate- day prednisone in myasthenia gravis
-
Warmolts JR, Engel WK. (1972) Benefit from alternate- day prednisone in myasthenia gravis. NEngl J Med 286, 17-20.
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(1972)
NEngl J Med
, vol.286
, pp. 17-20
-
-
Warmolts, J.R.1
Engel, W.K.2
-
12
-
-
0014934129
-
Alternate-day prednisone in a patient with myasthenia gravis
-
Warmolts JR, Engel WK, Whitaker JN. (1970) Alternate- day prednisone in a patient with myasthenia gravis. Lancet 2, 1198-1199.
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(1970)
Lancet
, vol.2
, pp. 1198-1199
-
-
Warmolts, J.R.1
Engel, W.K.2
Whitaker, J.N.3
-
13
-
-
0016915792
-
Myasthenia gravis, corticosteroids, anticholinesterases
-
Engel WK. (1976) Myasthenia gravis, corticosteroids, anticholinesterases. Ann NY Acad Sci 274, 623-630.
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(1976)
Ann NY Acad Sci
, vol.274
, pp. 623-630
-
-
Engel, W.K.1
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14
-
-
0035894609
-
Polyneuropathy in type 2 diabetes mellitus
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Engel WK. (2001) Polyneuropathy in type 2 diabetes mellitus. Lancet 358, 2086.
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(2001)
Lancet
, vol.358
, pp. 2086
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-
Engel, W.K.1
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15
-
-
0025985493
-
RNA metabolism in relation to amyotrophic lateral sclerosis
-
Engel WK. (1991) RNA metabolism in relation to amyotrophic lateral sclerosis. Adv Neurol 56, 125-153.
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(1991)
Adv Neurol
, vol.56
, pp. 125-153
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-
Engel, W.K.1
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16
-
-
0026072318
-
Does a retrovirus cause amyotrophic lateral sclerosis?
-
Engel WK. (1991) Does a retrovirus cause amyotrophic lateral sclerosis?. Ann Neurol 30, 431-433.
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(1991)
Ann Neurol
, vol.30
, pp. 431-433
-
-
Engel, W.K.1
-
17
-
-
13344257516
-
An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement
-
Engel WK, Kurland LT, Klatzo I. (1959) An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement. An intermediate form? Brain 82, 203-220.
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(1959)
An intermediate form? Brain
, vol.82
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-
Engel, W.K.1
Kurland, L.T.2
Klatzo, I.3
-
18
-
-
84885540536
-
In ALS, viral-dysmetabolic mechanisms acting via neuronal-nurturing cells (NNCs) could portend replacement therapy and should be sought by multi-tissue screening for rev-transcriptase (RT) and viral tracks
-
Engel WK. (2008) In ALS, viral-dysmetabolic mechanisms acting via neuronal-nurturing cells (NNCs) could portend replacement therapy and should be sought by multi-tissue screening for rev-transcriptase (RT) and viral tracks. Neuromuscul Disord 18, 764.
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Neuromuscul Disord
, vol.18
, pp. 764
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-
Engel, W.K.1
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19
-
-
38549107484
-
Quantification of reverse transcriptase in ALS and elimination of a novel retroviral candidate
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McCormick AL, Brown RH, Cudkowicz ME et al. (2008) Quantification of reverse transcriptase in ALS and elimination of a novel retroviral candidate. Neurology 70: 278-283.
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Neurology
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McCormick, A.L.1
Brown, R.H.2
Cudkowicz, M.E.3
-
20
-
-
84885488959
-
Liver-biopsy abnormalities in amyotropic lateral sclerosis
-
Engel WK, Patterson JM, Tauzin MR et al. (1988) Liver-biopsy abnormalities in amyotropic lateral sclerosis. Ann Neurol 24, 163.
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(1988)
Ann Neurol
, vol.24
, pp. 163
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-
Engel, W.K.1
Patterson, J.M.2
Tauzin, M.R.3
-
21
-
-
0001274692
-
Amyotrophic lateral sclerosis (ALS) associated with HTLV-I infection
-
Prentice A, Engel WK, Rasheed S. (1992) Amyotrophic lateral sclerosis (ALS) associated with HTLV-I infection. Neurology 42, 454-455.
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(1992)
Neurology
, vol.42
, pp. 454-455
-
-
Prentice, A.1
Engel, W.K.2
Rasheed, S.3
-
22
-
-
0024540096
-
High-dose TRH treatment of neuromuscular diseases: summary of Mechanisms and critique of clinical studies
-
Engel WK. (1989) High-dose TRH treatment of neuromuscular diseases: summary of Mechanisms and critique of clinical studies. Ann NY Acad Sci 553, 462-472.
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(1989)
Ann NY Acad Sci
, vol.553
, pp. 462-472
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-
Engel, W.K.1
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23
-
-
0020519116
-
Effect on weakness and spasticity in amyotrophic lateral sclerosis of thyrotropin-releasing hormone
-
Engel WK, Siddique T, Nicoloff JT. (1983) Effect on weakness and spasticity in amyotrophic lateral sclerosis of thyrotropin-releasing hormone. Lancet 2, 73-75.
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Lancet
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Engel, W.K.1
Siddique, T.2
Nicoloff, J.T.3
-
24
-
-
84885488922
-
Myophosphorylase deficiency (MPD) probably also involves lower motor neurons (LMNs) in some cases
-
Engel WK, Beydoun SR. (1985) Myophosphorylase deficiency (MPD) probably also involves lower motor neurons (LMNs) in some cases. Neurology 35, 304.
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(1985)
Neurology
, vol.35
, pp. 304
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-
Engel, W.K.1
Beydoun, S.R.2
-
25
-
-
33646699509
-
Introduction to disorders of the motor neuron, nerves and related abnormalities
-
Goldensohn ES, Appel SH (eds), Lea Febiger, Philadelphia
-
Engel WK. (1977) Introduction to disorders of the motor neuron, nerves and related abnormalities. In: Goldensohn ES, Appel SH (eds), Scientific Approaches to Clinical Neurology. Lea Febiger, Philadelphia, pp. 1250-1321.
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(1977)
Scientific Approaches to Clinical Neurology
, pp. 1250-1321
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-
Engel, W.K.1
-
26
-
-
77956357112
-
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia
-
Yan J, Deng HX, Siddique N et al. (2010) Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia. Neurology 75, 807-814.
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Neurology
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Yan, J.1
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27
-
-
0345438726
-
Fasciculating progressive muscular atrophy (F-PMA) remarkably responsive to anti-dysimmune treatment (ADIT)-a possible clue to more ordinary ALS?
-
Engel WK, Hopkins LC, Rosenberg BJ. (1985) Fasciculating progressive muscular atrophy (F-PMA) remarkably responsive to anti-dysimmune treatment (ADIT)-a possible clue to more ordinary ALS?. Neurology 35, 72.
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(1985)
Neurology
, vol.35
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-
Engel, W.K.1
Hopkins, L.C.2
Rosenberg, B.J.3
-
28
-
-
1542538141
-
Rapid and continued improvement from intravenous immunoglobulin treatment of asymmetrical chronic progressive muscular atrophy after 19 years of disease progression
-
Engel WK. (1995) Rapid and continued improvement from intravenous immunoglobulin treatment of asymmetrical chronic progressive muscular atrophy after 19 years of disease progression. Ann Neurol 38, 333-334.
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(1995)
Ann Neurol
, vol.38
, pp. 333-334
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-
Engel, W.K.1
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30
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-
33644850570
-
Inclusion-body myositis: clinical, diagnostic, and pathologic aspects
-
Engel WK, Askanas V. (2006) Inclusion-body myositis: clinical, diagnostic, and pathologic aspects. Neurology 66, S20-29.
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(2006)
Neurology
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Engel, W.K.1
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31
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-
0027240930
-
Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer's disease using fluorescence technique
-
Askanas V, Engel WK, Alvarez RB. (1993) Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer's disease using fluorescence technique. Neurology 43, 1265-1267.
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Neurology
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Askanas, V.1
Engel, W.K.2
Alvarez, R.B.3
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32
-
-
0017618256
-
Scanning for soft-tissue amyloid
-
Kula RW, Engel WK, Line BR. (1977) Scanning for soft-tissue amyloid. Lancet 1, 92-93.
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(1977)
Lancet
, vol.1
, pp. 92-93
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-
Kula, R.W.1
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Line, B.R.3
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33
-
-
33646708456
-
Plasma-cell dyscrasic amyloid neuropathy: a parasparafucile phenomenon?
-
Serratrice G, Roux H (eds), Masson Publishing Co, New York
-
Engel WK, Trotter JL. (1979) Plasma-cell dyscrasic amyloid neuropathy: a parasparafucile phenomenon?. In: Serratrice G, Roux H (eds), Peroneal Atrophies and Related Disorders. Masson Publishing Co, New York, pp. 339-347.
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Peroneal Atrophies and Related Disorders
, pp. 339-347
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-
Engel, W.K.1
Trotter, J.L.2
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35
-
-
84885489304
-
A simple, low-tech clinical test and treatment for cervical root compression
-
Engel WK. (1987) A simple, low-tech clinical test and treatment for cervical root compression. Ann Neurol 22, 165.
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(1987)
Ann Neurol
, vol.22
, pp. 165
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-
Engel, W.K.1
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37
-
-
0015513452
-
Vascular deposits of immunoglobin and complement in idiopathic inflammatory myopathy
-
Whitaker JN, Engel WK. (1972) Vascular deposits of immunoglobin and complement in idiopathic inflammatory myopathy. New Engl J Med 286, 333-338.
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(1972)
New Engl J Med
, vol.286
, pp. 333-338
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-
Whitaker, J.N.1
Engel, W.K.2
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38
-
-
0015921717
-
Mechanisms of muscle injury in idiopathic inflammatory myopathy
-
Whitaker JN, EngelWK. (1973) Mechanisms of muscle injury in idiopathic inflammatory myopathy. New Engl J Med 289, 107-108.
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New Engl J Med
, vol.289
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-
Whitaker, J.N.1
Engel, W.K.2
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39
-
-
0015219671
-
Duchenne muscular dystrophy: functional ischemia reproduces its characteristic lesions
-
Mendell JR, Engel WK, Derrer EC. (1970) Duchenne muscular dystrophy: functional ischemia reproduces its characteristic lesions. Science 172, 1143-1145.
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Science
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Mendell, J.R.1
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Derrer, E.C.3
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40
-
-
0015526126
-
Increased plasma enzyme concentrations in rats with functional ischemia of muscle provide a possible model of Duchenne muscular dystrophy
-
Mendell JR, Engel WK, Derrer EC. (1972) Increased plasma enzyme concentrations in rats with functional ischemia of muscle provide a possible model of Duchenne muscular dystrophy. Nature 239, 522-524.
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Nature
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Mendell, J.R.1
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41
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0001940664
-
Duchenne muscular dystrophy: a histologically based ischemia hypothesis and comparison with experimental ischemia myopathy
-
Pearson CM, Mostofi FK (eds), Williams&Wilkins Co, Baltimore
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Engel WK. (1973) Duchenne muscular dystrophy: a histologically based ischemia hypothesis and comparison with experimental ischemia myopathy. In: Pearson CM, Mostofi FK (eds), The Striated Muscle. Williams&Wilkins Co, Baltimore, vol. 12, pp. 453-472.
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The Striated Muscle
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Engel, W.K.1
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42
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3543054982
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Integrative histochemical approach to the defect of Duchenne muscular dystrophy
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Rowland LP (ed.), American Elsevier Publishing Co, New York, Excerpta Medica
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Engel WK. (1977) Integrative histochemical approach to the defect of Duchenne muscular dystrophy. In: Rowland LP (ed.), Pathogenesis of the Human Muscular Dystrophies, American Elsevier Publishing Co, New York, Excerpta Medica, pp. 277-309.
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Pathogenesis of the Human Muscular Dystrophies
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Engel, W.K.1
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43
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Drugs blocking the muscle-damaging effects of 5-HT and nonadrenaline in aorta-ligated rats
-
Engel WK, Derrer EC. (1975) Drugs blocking the muscle-damaging effects of 5-HT and nonadrenaline in aorta-ligated rats. Nature 254, 151-152.
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Nature
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44
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-
Monoclonal gammopathy of undetermined significance
-
Kyle RA. (1978) Monoclonal gammopathy of undetermined significance. Natural history in 241 cases. Am J Med 64, 814-826.
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Natural history in 241 cases. Am J Med
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-
Kyle, R.A.1
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45
-
-
0017526167
-
MB-creatine phosphokinase isoenzyme elevation not diagnostic of myocardial infarction
-
Adornato BT, Engel WK. (1977) MB-creatine phosphokinase isoenzyme elevation not diagnostic of myocardial infarction. Arch Intern Med 137, 1089-1090.
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Arch Intern Med
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Adornato, B.T.1
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46
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26844522790
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Correlation ofmotor unit behavior with histochemical and myofiber type in humans by open-biopsy electromyography
-
Desmedt JE (ed.), Karger, Basel
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Warmolts JR, EngelWK. (1973) Correlation ofmotor unit behavior with histochemical and myofiber type in humans by open-biopsy electromyography. In: Desmedt JE (ed.), New Developments in Electromyography and Clinical Neurophysiology, Karger, Basel, pp. 35-40.
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New Developments in Electromyography and Clinical Neurophysiology
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Warmolts, J.R.1
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48
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84948724649
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Introduction to the myopathies
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Goldensohn ES, Appel SH (eds), Lea Febiger, Philadelphia
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Engel WK. (1977) Introduction to the myopathies. In: Goldensohn ES, Appel SH (eds), Scientific Approaches to Clinical Neurology, Lea Febiger, Philadelphia, pp. 1602-1632.
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Scientific Approaches to Clinical Neurology
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Engel, W.K.1
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49
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0015940282
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"Myopathic EMG" -nonesuch animal
-
Engel WK. (1973) "Myopathic EMG" -nonesuch animal. New Engl J Med 289, 485-486.
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New Engl J Med
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Engel, W.K.1
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50
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Brief, small, abundant motor-unit action potentials
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Engel WK. (1975) Brief, small, abundant motor-unit action potentials. Neurology 25, 173-176.
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Neurology
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51
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Correlative histochemical study of skeletal muscle after a suprasegmental denervation, peripheral nerve section, and skeletal fixation
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Karpati G, EngelWK. (1968) Correlative histochemical study of skeletal muscle after a suprasegmental denervation, peripheral nerve section, and skeletal fixation. Neurology 18, 681-692.
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Neurology
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Karpati, G.1
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52
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0014236649
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Histochemical investigation of fiber type ratios with the myofibrillar ATPase reaction in normal and denervated skeletal muscles in guinea pig
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Karpati G, Engel WK. (1968) Histochemical investigation of fiber type ratios with the myofibrillar ATPase reaction in normal and denervated skeletal muscles in guinea pig. Am J Anat 122, 145-155.
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Am J Anat
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Karpati, G.1
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53
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0014413462
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Acetazolamide prophylaxis in hypokalemic periodic paralysis
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Resnick JS, Engel WK, Griggs RC et al. (1968) Acetazolamide prophylaxis in hypokalemic periodic paralysis. N Engl J Med 278, 582-586.
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N Engl J Med
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54
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Acetazolamide treatment of hypokalemic periodic paralysis
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Griggs RC, Engel WK, Resnick JS. (1970) Acetazolamide treatment of hypokalemic periodic paralysis. Ann Intern Med 73, 39-48.
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Ann Intern Med
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Griggs, R.C.1
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55
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0020582252
-
Treatment of "permanent" muscle weakness in familial hypokalemic periodic paralysis
-
Dalakas MC, Engel WK. (1983) Treatment of "permanent" muscle weakness in familial hypokalemic periodic paralysis. Muscle Nerve 6, 182-186.
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Muscle Nerve
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Dalakas, M.C.1
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56
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84885546279
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Toxicity of long-chain fatty acids (LCFAs) in muscle carnitine deficiency and other LCFA endodissolutions? Dietary LCFA restriction associated with dramatic long-term improvement
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Askanas V, Engel WK. (2003) Toxicity of long-chain fatty acids (LCFAs) in muscle carnitine deficiency and other LCFA endodissolutions? Dietary LCFA restriction associated with dramatic long-term improvement. Neurology 36, 94.
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Neurology
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Toxic role of long-chain fattyacids in muscle carnitine deficiency and other LCFA endodissolutions: dietary LCFA retriction associated with dramatic long-term improvement
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Engel, WK. (1986) Toxic role of long-chain fattyacids in muscle carnitine deficiency and other LCFA endodissolutions: dietary LCFA retriction associated with dramatic long-term improvement. Neurology 36 (Suppl 1), 94.
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Neurology
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58
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0021952576
-
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free diet
-
Askanas V, Engel WK, Kwan HH et al. (1985) Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free diet. Neurology 35, 66-72.
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Neurology
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59
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Nearly fatal muscle carnitine deficiency with full recovery after replacement therapy
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Prockop LD, Engel WK, Shug AL. (1983) Nearly fatal muscle carnitine deficiency with full recovery after replacement therapy. Neurology 33, 1629-1631.
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Motor neuron histochemistry in ALS and infantile spind muscular a trophy
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