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HHDHeavy Heavy Duty
HHDHealth and Human Development (Education Development Center, Inc.)
HHDHerbert Hoover Dike (Florida)
HHDHusker Harvest Days (trade show; Nebraska)
HHDHeadquarters Detachment
HHDHybrid Hard Drive (Samsung/Microsoft)
HHDHailey-Hailey Disease
HHDHand Held Device
HHDHypertensive Heart Disease (cardiovascular disorder)
HHDHeadquarters & Headquarters Detachment
HHDHip Hop Discussion (forum)
HHDHappy Hump Day
HHDHartford Health Department
HHDHylian Help Desk (website)
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References in periodicals archive ?
Tawfik pointed out that the trade-off in the financial offers will focus on the percentage that the management company will receive annually from HHD capital for management services.
Neiltje gets most enthusiastic when she talks about her latest project with HDU: a three-year research project designed to identify barriers in HHD that cause the alarmingly high drop off rate from the modality (Weinhandl & Collins 2018).
[42.] Reiter M, Pfaffl MW Schonfelder M, Meyer HHD. Gene expression in hair follicle dermal papilla cells after treatment with stanozolol.
Recent developments in Medicare's dialysis reimbursement policies make providing HHD therapy still more attractive.
Some of the physical benefits of nocturnal HHD were seen in this INHD population.
From the previously cited studies, operator's inefficiency to hold the HHD in the right position emerged as the main issue in HHD strength measurements related to the ankle joint.
In HHD, heterozygous mutation of calcium dependent ATP2C1 gene (chromosome 3q21-24) is seen which results in dysfunction of a Golgi-associated Ca2+ ATPase and interferes with intracellular Ca2+ signaling.2
The average score for HHH was 1.9 [+ or -] 0.4,1.8 [+ or -] 0.5 for HHC, 1.7 [+ or -] 0.5 for HHMO, 1.7 [+ or -] 0.5 for HHD, and 1.5 [+ or -] 0.7 for TINA.
This proves most challenging in the HHD program where each home can have differing qualities of potable water.
INTRODUCTION: Hailey-Hailey disease (HHD) is a rare autosomal dominant acantholytic disorder which recurs with remitting and relapsing episodes.[1] The defect in ATPC2 gene leads to calcium channel dysfunction which results in defect in epidermis.