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PubPharm (24)
1
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex Dystonia
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Khan, A.
|
Molitor, A.
|
Mayeur, S.
| +11
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2
Unnecessary Use of Corticosteroids for managing early mild symptoms of COVID-19 may lead to Rhino-ortibal-cerebral mucormycosis in Patients with Diabetes - a case series from Lahore, Pakistan
enthalten in:
Therapeutic advances in infectious disease
| 2022
von
Iqtadar, S.
|
Hashmat, M.
|
Chaudhry, M.
| +4
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3
Colchicine in Recently Hospitalized Patients with COVID-19 : A Randomized Controlled Trial (COL-COVID)
enthalten in:
International journal of general medicine
| 2021
von
Pascual-Figal, D.
|
Roura-Piloto, A.
|
Moral-Escudero, E.
| +12
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4
Possible Therapeutic Effects of Adjuvant Quercetin Supplementation Against Early-Stage COVID-19 Infection : A Prospective, Randomized, Controlled, and Open-Label Study
enthalten in:
International journal of general medicine
| 2021
von
Di Pierro, F.
|
Derosa, G.
|
Maffioli, P.
| +16
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5
Potential Clinical Benefits of Quercetin in the Early Stage of COVID-19 : Results of a Second, Pilot, Randomized, Controlled and Open-Label Clinical Trial
enthalten in:
International journal of general medicine
| 2021
von
Di Pierro, F.
|
Iqtadar, S.
|
Khan, A.
| +9
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6
NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation
enthalten in:
The Journal of experimental medicine
| 2020
von
Castro, C.
|
Rosenzwajg, M.
|
Carapito, R.
| +29
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7
Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants
enthalten in:
Genes
| 2020
von
Khan, A.
|
Miao, Z.
|
Umair, M.
| +7
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8
Biallelic variants in four genes underlying recessive osteogenesis imperfecta
enthalten in:
European journal of medical genetics
| 2020
von
Hayat, A.
|
Hussain, S.
|
Bilal, M.
| +15
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9
Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia : a case report
enthalten in:
BMC pulmonary medicine
| 2020
von
Al Mutairi, F.
|
Alkhalaf, R.
|
Alkhorayyef, A.
| +11
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10
A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome
enthalten in:
Chinese medical journal
| 2019
von
Yu, X.
|
Wang, R.
|
Han, S.
| +7
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Thema: Case Reports
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24
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3
International journal of general medicine
3
Journal of Ayub Medical College, Abbottabad : JAMC
3
Journal of the College of Physicians and Surgeo...
2
BMJ case reports
2
Frontiers in pediatrics
1
American journal of medical genetics. Part A
1
Archives of disease in childhood. Education and...
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Thema
Case Reports
16
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4
Research Support, Non-U.S. Gov't
3
Klinische Studie
2
Biomarkers, Tumor
2
COVID-19
2
Pakistani family
2
SARS-CoV-2
2
coronavirus
1
11056-06-7
1
144351-15-5
1
5V9KLZ54CY
1
75J73V1629
1
7GR28W0FJI
1
80168379AG
1
ARHGAP31 protein, human
1
Actins
1
Acyclovir
1
Adaptor Proteins, Signal Transducing
1
Albuterol
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Erscheinungszeitraum
9
2020-
14
2010-2019
1
2000-2009
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