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New England Journal of Medicine
Research Hotspot & Journal Scope - Progressive

New England Journal of Medicine - DOI: 10.1056/NEJMicm1809675
Chronic Silicosis with Progressive Massive Fibrosis.

Leonard Riley · Daniel Urbine ·

New England Journal of Medicine - DOI: 10.1056/NEJMcpc1900143
Case 10-2019: A 69-Year-Old Man with Progressive Dyspnea.

Katharine E Black · Sydney B Montesi · Jennifer F Feneis · Eugene J Mark ·


She had progressive dyspnea, chest pain and hypotension.

Very rare and serious complication of central line insertion [10.18231/j.ijca.2019.121]

There was a significant increase in the disability level in 2007, with a progressive decline to 2011 and a gradual decline to 2017.

Dynamics and Structure of Primary Disability in Retirement-Age Citizens Applying to the Bureau of Medical and Social Expertise of St. Petersburg in 2006–2017 [10.1134/S2079057019010089]

Our results indicate that the three pathogenic variants, two of which were novel, underlie AD-COD/CORD with progressive retinal atrophy, and the prevalence (0.

Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophies [10.1038/s41598-019-52660-1]

, attributed to TOR1A, THAP1, GNAL, and ANO3 mutations) is that of a gradual onset of dystonia which often spreads, but then follows a stable disease course once signs are established (typically over a few years), it is noteworthy that there was a clearly progressive course over 30 years in 1 patient and more subtle progression in three others.

Delineating the phenotype of autosomal‐recessive HPCA mutations: Not only isolated dystonia! [10.1002/mds.27638]

Spinocerebellar ataxia type 2 (SCA2) is a rare disease characterized by slowly progressive ataxia, dysarthria, ophthalmoplegia, and slow saccade.

Spinocerebellar ataxia type 2 presenting with involuntary movement: a diagnostic dilemma [10.1177/0300060519889457]

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