Results 181 to 190 of about 101,913 (345)

Towards model predictive control: online predictions of ammonium and nitrate removal by using a stochastic ASM [PDF]

open access: bronze, 2018
Peter Alexander Stentoft   +5 more
openalex   +1 more source

ASMS News

open access: yesJournal of the American Society for Mass Spectrometry, 1995
openaire   +1 more source

Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2‐developmental and epileptic encephalopathy

open access: yesEpilepsia, EarlyView.
Overview of the multimodal experimental approach integrating clinical, genetic, in silico, and in vitro investigations. Clinical: Representative EEG recording setup and ictal traces from affected patients. Genetic: Pedigrees for Families A and B highlighting the inheritance of the four identified SLC12A5 variants (A1, A2, B1, B2).
Mira Hamze   +19 more
wiley   +1 more source

Founders of the Moldovian Academy of Sciences. Encyclopedic approach

open access: yesЕнциклопедичний Вісник України, 2015
Konstantin Manolache, Ion Xenofontov
doaj   +1 more source

Dietary Branched-Chain Amino Acid Intake Is Associated with Muscle Mass and Handgrip Strength: Evidence from China-Health and Nutrition Survey 2015-2024. [PDF]

open access: yesNutrients
Xu Z   +15 more
europepmc   +1 more source

A Systematic Search for Periodicities inRXTEASM Data [PDF]

open access: bronze, 2006
L. Wen   +3 more
openalex   +1 more source

Management of ring chromosome 20 syndrome: Narrative review and consensus recommendations

open access: yesEpilepsia, EarlyView.
Abstract Ring chromosome 20 (ring 20) is a rare genetic condition usually presenting as developmental and epileptic encephalopathy. The disease is caused by fusion of the long and short arms of chromosome 20. Patients are symptomatic even if there is no loss of genetic material.
Asma Khamis   +8 more
wiley   +1 more source

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