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1. Full Text Can we turn mice into men?
by Ludolph, Albert C
Journal of Neurochemistry, ISSN 0022-3042, 04/2019, Volume 149, Issue 2, pp. 168 - 169
The pressure to develop pharmacological therapeutic interventions in the field of the rapidly progressing, fatal disease amyotrophic lateral sclerosis (ALS) is... 
Neuroprotection | Cannabinoids | Therapeutic applications | Amyotrophic lateral sclerosis | Systematic review | Mice | Pharmacology | Inflammation | Neuroprotective agents
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2. Full Text Therapeutic advances in SMA
by Ludolph, Albert C and Wurster, Claudia D
Current opinion in neurology, ISSN 1350-7540, 08/2019, Volume 32, Issue 5, pp. 777 - 781
To review the advent of novel therapies and their impact on the field of chromosome 5q-associated spinal muscular atrophy (SMA). Antisense oligonucleotides... 
Drug therapy | Genetic aspects | Spinal muscular atrophy
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3. Retinoids and Amyotrophic Lateral Sclerosis/Reply
by Gabriele Nagel and Dietrich Rothenbacher and Albert C Ludolph
JAMA Neurology, ISSN 2168-6149, 09/2018, Volume 75, Issue 9, p. 1153
Nagel et al replies on the comments of Riancho et al on their article that investigate the association of retinol-binding protein 4 (RBP4) concentrations with... 
Proteins | Vitamin A | Clinical aspects | Medical prognosis | Amyotrophic lateral sclerosis | Retinoids | Risk factors | Retinol-binding protein
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4. Amyotrophe Lateralsklerose
by Dengler, Reinhard and Ludolph, Albert C and Zierz, S and Karitzky, Jochen
2000, 2. umfassend überarbeitete und erw. Aufl., ISBN 9783131275028, x, 146
Amyotrophic lateral sclerosis
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5. Full Text Motor neuron disease: Genetic testing in amyotrophic lateral sclerosis
by Ludolph, Albert C
Nature reviews. Neurology, ISSN 1759-4758, 05/2017, Volume 13, Issue 5, p. 262
Frontotemporal Dementia - genetics | Amyotrophic Lateral Sclerosis - diagnosis | Genetic Testing - economics | Frontotemporal Dementia - diagnosis | Amyotrophic Lateral Sclerosis - genetics | Humans | Amyotrophic lateral sclerosis | Genetic aspects | Diagnosis | Research | Analysis | Genetic screening
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6. Full Text Braak staging in clinical practice?
by Ludolph, Albert C
Neurology, ISSN 0028-3878, 03/2014, Volume 82, Issue 10, p. 862
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7. Full Text Genetic testing in amyotrophic lateral sclerosis
by Ludolph, AC
NATURE REVIEWS NEUROLOGY, ISSN 1759-4758, 05/2017, Volume 13, Issue 5, pp. 262 - 263
A new survey of clinicians from 21 different countries has found a lack of consensus regarding the definition of familial amyotrophic lateral sclerosis. In... 
CLINICAL NEUROLOGY | FRONTOTEMPORAL DEMENTIA
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8. Full Text Intrathecal administration of nusinersen in adolescent and adult SMA type 2 and 3 patients
by Wurster, Claudia D and Winter, Benedikt and Wollinsky, Kurt and Ludolph, Albert C and Uzelac, Zeljko and Witzel, Simon and Schocke, Michael and Schneider, Ralf and Kocak, Tugrul
Journal of Neurology, ISSN 0340-5354, 1/2019, Volume 266, Issue 1, pp. 183 - 194
Spinal muscular atrophy is a genetic motor neuron disease that leads to progressive muscular atrophy and muscle weakness. In December 2016, the Food and Drug... 
Neurology | Neurosciences | Medicine & Public Health | Nusinersen | Neuroradiology | Lumbar puncture | Spinal muscular atrophy | DIAGNOSIS | MANAGEMENT | SPINAL MUSCULAR-ATROPHY | CLINICAL NEUROLOGY | PUNCTURE | Injections, Spinal | Spinal Puncture | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Treatment Outcome | Spinal Muscular Atrophies of Childhood - diagnostic imaging | Spinal Muscular Atrophies of Childhood - therapy | Young Adult | Adolescent | Adult | Female | Biological Products - administration & dosage | Oligonucleotides - administration & dosage | Child | CT imaging | Care and treatment | Usage | Neurons | Genetic aspects | Research | Atrophy | Motor neuron diseases | Scoliosis | Spine (lumbar) | Antisense oligonucleotides | Anesthesia | Cerebrospinal fluid | Patients
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9. Neurodegenerative Erkrankungen
by Ludolph, Albert C
Klinikarzt, ISSN 0341-2350, 2018, Volume 47, Issue 10, pp. 442 - 443
Journal Article
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10. Full Text Can we turn mice into men? An Editorial for 'Effects of cannabinoids in Amyotrophic Lateral Sclerosis (ALS) murine models: a systematic review and meta-analysis' page 284
by Ludolph, AC
JOURNAL OF NEUROCHEMISTRY, ISSN 0022-3042, 04/2019, Volume 149, Issue 2, pp. 168 - 169
The pressure to develop pharmacological therapeutic interventions in the field of the rapidly progressing, fatal disease amyotrophic lateral sclerosis (ALS) is... 
NEUROSCIENCES | BIOCHEMISTRY & MOLECULAR BIOLOGY | Phenols | Amyotrophic lateral sclerosis
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11. Full Text Differential diagnosis of peripheral facial nerve palsy: a retrospective clinical, MRI and CSF-based study
by Zimmermann, Julia and Jesse, Sarah and Kassubek, Jan and Pinkhardt, Elmar and Ludolph, Albert C
Journal of Neurology, ISSN 0340-5354, 10/2019, Volume 266, Issue 10, pp. 2488 - 2494
Facial nerve palsy is the most common cranial nerve disorder. There is no consensus on a single diagnostic tool deemed as the ‘gold standard’ for... 
Neurology | Neurosciences | Medicine & Public Health | Facial paralysis | Neuroborreliosis | Cerebrospinal fluid | Etiologies | MR-imaging | Neuroradiology | Ramsay-Hunt-Syndrome | Facial nerve palsy | Lyme disease | Nuclear magnetic resonance--NMR | Central nervous system | Borreliosis | Facial nerve | Infections | Inflammation | Patients | Magnetic resonance imaging | Cranial nerves | Differential diagnosis | Paralysis | Autoimmune diseases | Neurological disorders
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12. Full Text Corticoefferent pathology distribution in amyotrophic lateral sclerosis: in vivo evidence from a meta-analysis of diffusion tensor imaging data
by Gorges, Martin and Del Tredici, Kelly and Dreyhaupt, Jens and Braak, Heiko and Ludolph, Albert C and Müller, Hans-Peter and Müller, Hans-Peter and Kassubek, Jan
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 15389 - 10
A sequential transaxonal disease spread of amyotrophic lateral sclerosis (ALS)-associatedTDP-43 pathology in four stages has been defined by post-mortem data,... 
MOTOR-NEURON DISEASES | PATTERNS | PTDP-43 PATHOLOGY | TDP-43 | MULTIDISCIPLINARY SCIENCES | BRAIN | Neuroimaging | Image processing | Cortex | Data processing | Amyotrophic lateral sclerosis | Pyramidal tracts | Substantia alba | Disease spread | Pathology | Magnetic resonance imaging | Autopsy | Anisotropy | Hippocampus
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13. Full Text Juxtacortical lesions are associated with seizures in cerebral small vessel disease
by Stösser, Sebastian and Böckler, Stefanie and Ludolph, Albert C and Kassubek, Jan and Neugebauer, Hermann
Journal of Neurology, ISSN 0340-5354, 5/2019, Volume 266, Issue 5, pp. 1230 - 1235
Small vessel cerebrovascular disease (SVCD) can manifest with epileptic seizures and transient ischemic attacks (TIA). This study was designed to test if the... 
Neurology | Neurosciences | Transient ischemic attack | Medicine & Public Health | Magnetic resonance imaging | Cerebral small vessel diseases | Neuroradiology | Seizures | STROKE | MICROINFARCT BURDEN | TEMPORAL-LOBE ATROPHY | DEFICITS | OCCLUSION | CLINICAL NEUROLOGY | Temporal lobe | Nuclear magnetic resonance--NMR | Epilepsy | Substantia alba | Multivariate analysis | Atrophy | Convulsions & seizures | Spatial distribution | Vascular diseases | Ischemia | Cardiovascular diseases | Cerebrovascular diseases | Geriatrics
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14. Full Text Non‐invasive ventilation and hypercapnia‐associated symptoms in amyotrophic lateral sclerosis
by Dorst, Johannes and Behrendt, Georg and Ludolph, Albert C
Acta Neurologica Scandinavica, ISSN 0001-6314, 02/2019, Volume 139, Issue 2, pp. 128 - 134
Objectives During the course of amyotrophic lateral sclerosis (ALS), progressive weakness of respiratory muscles leads to chronic hypercapnia which causes... 
respiratory symptoms | Amyotrophic Lateral Sclerosis | non‐invasive ventilation | hypercapnia | non-invasive ventilation | SURVIVAL | SLEEP | DISEASE | QUALITY-OF-LIFE | SCALE | CLINICAL NEUROLOGY | Hypercapnia | Sleep | Hypoventilation | Daytime | Muscles | Ventilation | Amyotrophic lateral sclerosis | Fatigue | Sleep and wakefulness | Quality of life
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15. Full Text Short-term and long-term effects of immunoadsorption in refractory chronic inflammatory demyelinating polyneuropathy: a prospective study in 17 patients
by Dorst, Johannes and Ludolph, Albert C and Senel, Makbule and Tumani, Hayrettin
Journal of Neurology, ISSN 0340-5354, 12/2018, Volume 265, Issue 12, pp. 2906 - 2915
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare, autoimmune-inflammatory disease of the peripheral nervous system. Recently, various... 
Neurology | Neurosciences | Medicine & Public Health | Immunoadsorption | CIDP | Neuroradiology | Chronic inflammatory demyelinating polyneuropathy | Long-term effects | PLASMA-EXCHANGE | POLYRADICULONEUROPATHY | CLINICAL NEUROLOGY | Prospective Studies | Immunoglobulin G - blood | Humans | Middle Aged | Male | Treatment Outcome | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - physiopathology | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - therapy | Time Factors | Immunotherapy | Female | Aged | Muscle Strength | Care and treatment | Usage | Polyneuropathies | Diagnosis | Research | Methods | Immunoglobulins | Autoantibodies | Intravenous administration | Demyelination | Immunoglobulin G | Nervous system | Immunoglobulin G4 | Muscular strength | Polyneuropathy | Patients | Steroid hormones
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16. Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
by Axel Freischmidt and Kathrin Müller and Albert C Ludolph
JAMA Neurology, ISSN 2168-6149, 01/2017, Volume 74, Issue 1, p. 110
  Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are related neurodegenerative syndromes that occur sporadically or have been associated... 
Proteins | Amyotrophic lateral sclerosis | Amino acids | Mutation | Ribonucleic acid--RNA | Dementia
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17. Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
by Freischmidt, Axel and Mueller, Kathrin and Ludolph, Albert C
JAMA Neurology, ISSN 2168-6149, 01/2017, Volume 74, Issue 1, pp. 110 - 110
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are related neurodegenerative syndromes that occur sporadically or have been associated... 
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18. Full Text Comment: Braak staging in clinical practice?
by Ludolph, Albert C
Neurology, ISSN 0028-3878, 03/2014, Volume 82, Issue 10, pp. 862 - 862
Parkinson Disease - pathology | Submandibular Gland - pathology | Humans | Lewy Body Disease - pathology | Submandibular Gland - metabolism | Brain - pathology | Female | Male | Parkinson Disease - metabolism | Biopsy, Needle - methods | Lewy Bodies - pathology | alpha-Synuclein - metabolism
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19. Full Text Prophylactic antibiotics to reduce pneumonia after acute stroke
by Neugebauer, Hermann and Lindner-Pfleghar, Beate and Jüttler, Eric and Ludolph, Albert C and Riecker, Axel
Lancet, The, ISSN 0140-6736, 2016, Volume 387, Issue 10017, pp. 432 - 433
  We read the Article by Lalit Kalra and colleagues with great interest but are concerned about some issues. In our opinion, STROKE-INF was a negative trial... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | Deglutition Disorders - complications | Pneumonia, Aspiration - prevention & control | Humans | Antibiotic Prophylaxis - methods | Stroke - complications | Female | Male | Stroke (Disease) | Pneumonia | Antibiotics | Drug therapy | Bacterial pneumonia | Stroke | Dysphagia | Endoscopy | Preventive medicine
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20. Full Text Non-invasive ventilation in amyotrophic lateral sclerosis
by Dorst, Johannes and Ludolph, Albert C
Therapeutic Advances in Neurological Disorders, ISSN 1756-2856, 06/2019, Volume 12, p. 1756286419857040
Non-invasive ventilation (NIV) has become an important cornerstone of symptomatic treatment in amyotrophic lateral sclerosis (ALS), improving survival and... 
motor neuron diseases | amyotrophic lateral sclerosis | non-invasive ventilation | SLOW VITAL CAPACITY | NOCTURNAL HYPOVENTILATION | FACTORS PREDICTING SURVIVAL | PULMONARY-FUNCTION | MOTOR-NEURON DISEASE | ALS PATIENTS | CLINICAL NEUROLOGY | PERCUTANEOUS ENDOSCOPIC GASTROSTOMY | MECHANICAL INSUFFLATION-EXSUFFLATION | QUALITY-OF-LIFE | RESPIRATORY INSUFFICIENCY
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