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H Jalali Selected Research

autosomal recessive Spastic paraplegia 20

1/2020A novel missense mutation (c.1006C>T) of SPG20 gene associated with Troyer syndrome.

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H Jalali Research Topics

Disease

1autosomal recessive Spastic paraplegia 20
01/2020
1Hereditary Spastic Paraplegia
01/2020
1Acquired Immunodeficiency Syndrome (AIDS)
11/2013
1Hyperalgesia
11/2013
1Neuralgia (Stump Neuralgia)
11/2013
1Cardiac Arrhythmias (Arrythmia)
05/2004
1Tetralogy of Fallot (Fallot Tetralogy)
10/2000
1Atrial Fibrillation
10/2000
1Transposition of Great Vessels (Great Vessels Transposition)
06/2000
1Aortic Dissection
06/2000

Drug/Important Bio-Agent (IBA)

1Proteins (Proteins, Gene)FDA Link
01/2020
1DNA (Deoxyribonucleic Acid)IBA
01/2020
1Nerve Growth Factor (NGF)IBA
11/2013
1CalciumIBA
11/2013
1Messenger RNA (mRNA)IBA
11/2013
1phospholambanIBA
10/2000
1Troponin IIBA
10/2000
1AnticoagulantsIBA
10/2000
1Formaldehyde (Formol)FDA Link
06/2000
1GelatinIBA
06/2000
1resorcinol (resorcin)IBA
06/2000
1Adhesives (Glues)IBA
06/2000

Therapy/Procedure

1Critical Care (Surgical Intensive Care)
05/2004