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PLAYING DEFENSE AGAINST LOU GEHRIG'S DISEASE.

Authors : Aebischer, Patrick¹; Kato, Ann C.²

Source: Scientific American. Nov2007, Vol. 297 Issue 5, p86-93. 8p.

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Academic Journal

Clinical presentation and diagnosis of Amyotrophic Lateral Sclerosis.

Authors : Ferguson, Toby A.¹; Elman, Lauren B.¹

Source: NeuroRehabilitation. 2007, Vol. 22 Issue 6, p409-416. 8p. 1 Diagram, 4 Charts.

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Diagnostic and therapeutic methods in the management of dysphagia in the ALS population: Issues in efficacy for the out-patient setting.

Authors : Palovcak, Merisa¹ ; Mancinelli, James M.²; Elman, Lauren B.¹

Source: NeuroRehabilitation. 2007, Vol. 22 Issue 6, p417-423. 7p. 3 Charts.

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Academic Journal

Neuropsychiatric features of Amyotrophic Lateral Sclerosis.

Authors : Elman, Lauren B.¹ ; Grossman, Murray²

Source: NeuroRehabilitation. 2007, Vol. 22 Issue 6, p425-429. 5p.

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Academic Journal

Nutrition throughout the course of ALS.

Authors : Golaszewski, Ame¹

Source: NeuroRehabilitation. 2007, Vol. 22 Issue 6, p431-434. 4p.

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Academic Journal

The role of physical therapy and occupational therapy in the treatment of Amyotrophic Lateral Sclerosis.

Authors : Lewis, Michele¹ ; Rushanan, Scott¹

Source: NeuroRehabilitation. 2007, Vol. 22 Issue 6, p451-461. 11p.

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Academic Journal

Amyotrophic Lateral Sclerosis: Ethical issues from diagnosis to end of life.

Authors : McCluskey, Leo¹

Source: NeuroRehabilitation. 2007, Vol. 22 Issue 6, p463-472. 10p. 1 Chart.

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Coexistence of amyotrophic lateral sclerosis and argyrophilic grain disease: A non-demented autopsy case showing circumscribed temporal atrophy and involvement of the amygdala.

Authors : Yokota, Osamu^1,2 ; Tsuchiya, Kuniaki^1,3,4; Noguchi, Yoshimasa⁵

Source: Neuropathology. Dec2007, Vol. 27 Issue 6, p539-550. 12p. 1 Black and White Photograph, 4 Diagrams, 2 Charts.

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ALS: astrocytes take center stage, but must they share the spotlight?

Authors : Knott, A. B.¹; Bossy-Wetzel, E.¹

Source: Cell Death & Differentiation. Dec2007, Vol. 14 Issue 12, p1985-1988. 4p.

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Comparative proteomic profiling of cerebrospinal fluid between living and post mortem ALS and control subjects.

Authors : Ranganathan, Srikanth¹ (AUTHOR); Nicholl, Georgina C. B.² (AUTHOR); Henry, Sarah² (AUTHOR)

Source: Amyotrophic Lateral Sclerosis. Dec2007, Vol. 8 Issue 6, p373-379. 7p. 3 Graphs.

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فلترة النتائج

PLAYING DEFENSE AGAINST LOU GEHRIG'S DISEASE.

Clinical presentation and diagnosis of Amyotrophic Lateral Sclerosis.

Diagnostic and therapeutic methods in the management of dysphagia in the ALS population: Issues in efficacy for the out-patient setting.

Neuropsychiatric features of Amyotrophic Lateral Sclerosis.

Nutrition throughout the course of ALS.

The role of physical therapy and occupational therapy in the treatment of Amyotrophic Lateral Sclerosis.

Amyotrophic Lateral Sclerosis: Ethical issues from diagnosis to end of life.

Coexistence of amyotrophic lateral sclerosis and argyrophilic grain disease: A non-demented autopsy case showing circumscribed temporal atrophy and involvement of the amygdala.

ALS: astrocytes take center stage, but must they share the spotlight?

Comparative proteomic profiling of cerebrospinal fluid between living and post mortem ALS and control subjects.

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