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1. Amyotrophic Lateral Sclerosis: Se origina cuando las células del sistema nervioso llamadas motoneuronas disminuyen gradualmente su funcionamiento y mueren, con lo que se provoca una parálisis muscular progresiva de pronóstico mortal: en sus etapas avanzadas, los pacientes sufren una parálisis total que se ... [100%] 2023-05-17
2. Amyotrophic lateral sclerosis: Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease, is a neurodegenerative disease that results in the progressive loss of motor neurons that control voluntary muscles. ALS is the most common type of ... (Neurodegenerative disease) [100%] 2021-12-23 [Amyotrophic lateral sclerosis] [Motor neuron diseases]...
3. Primary lateral sclerosis: Primary lateral sclerosis (PLS) is a very rare neuromuscular disease characterized by progressive muscle weakness in the voluntary muscles. PLS belongs to a group of disorders known as motor neuron diseases. [100%] 2023-10-25 [Motor neuron diseases] [Systemic atrophies primarily affecting the central nervous system]...
4. Primary lateral sclerosis: Primary lateral sclerosis (PLS) is a very rare neuromuscular disease characterized by progressive muscle weakness in the voluntary muscles. PLS belongs to a group of disorders known as motor neuron diseases. (Medicine) [100%] 2023-12-12 [Motor neuron diseases] [Rare diseases]...
5. Amyotrophic lateral sclerosis: Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease, is a neurodegenerative disease that results in the progressive loss of motor neurons that control voluntary muscles. ALS is the most common type of ... (Medicine) [100%] 2021-12-22 [Rare diseases] [Wikipedia medicine articles ready to translate]...
6. Amyotrophic lateral sclerosis (patient information): For the WikiDoc page for this topic, click here Overview What are the symptoms? What are the causes?. (Patient information) [100%] 2023-06-24 [For review] [Overview complete]...
7. Amyotrophic lateral sclerosis: Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease, is a disease that causes the death of neurons that control voluntary muscles. Some also use the term motor neuron disease for a group ... (Neurodegenerative disease characterized by progressive muscular weakness) [100%] 2023-10-28 [Amyotrophic lateral sclerosis] [Motor neuron diseases]...
8. Sclerosis: Sclerosis (from Greek σκληρός sklērós, "hard") is the stiffening of a tissue or anatomical feature, usually caused by a replacement of the normal organ-specific tissue with connective tissue. The structure may be said to have undergone sclerotic changes or display ... (Medicine) [93%] 2023-12-04 [Medical terminology]
9. Juvenile primary lateral sclerosis: Juvenile primary lateral sclerosis, also known as primary lateral sclerosis (PLSJ), is a very rare genetic disorder, with a small number of reported cases, characterized by progressive weakness and stiffness of muscles in the arms, legs, and face. The disorder ... (Medicine) [86%] 2023-10-02 [Autosomal recessive disorders] [Motor neuron diseases]...
10. Amyotrophic lateral sclerosis pathophysiology: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [86%] 2023-05-17 [Motor neuron disease] [Neurology]...
11. Amyotrophic lateral sclerosis surgery: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [86%] 2023-03-22 [(name of the system)]
12. Juvenile primary lateral sclerosis: Juvenile primary lateral sclerosis , also known as primary lateral sclerosis (PLSJ), is a very rare genetic disorder, with a small number of reported cases, characterized by progressive weakness and stiffness of muscles in the arms, legs, and face. The disorder ... [86%] 2023-11-07 [Systemic atrophies primarily affecting the central nervous system] [Autosomal recessive disorders]...
13. Lateral: Lateral hace referencia a varios artículos. [79%] 2023-09-01
14. Amyotrophic lateral sclerosis medical therapy: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [77%] 2023-07-26 [Motor neuron disease] [Neurology]...
15. Amyotrophic lateral sclerosis primary prevention: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [77%] 2023-03-25
16. Amyotrophic lateral sclerosis CT scan: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [77%] 2023-04-29 [(Name of the system)]
17. Amyotrophic lateral sclerosis historical perspective: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [77%] 2023-03-26 [(name of the system)]
18. Amyotrophic lateral sclerosis laboratory findings: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Amyotrophic lateral sclerosis from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Fi. [77%] 2023-03-22 [(name of the system)]
19. Splenosis: Articles Most recent articles on Splenosis Most cited articles on Splenosis Review articles on Splenosis Articles on Splenosis in N Eng J Med, Lancet, BMJ Media Powerpoint slides on Splenosis Images of Splenosis Photos of Splenosis Podcasts & MP3s on Splenosis ... [72%] 2023-12-21
20. Sclerostin: Sclerostin is a protein that in humans is encoded by the SOST gene. Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma ... [72%] 2023-12-26 [Human proteins] [Osteopathies]...