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Results for S in English, page 92
sedatively
Sedatives
Sedatives and Hypnotics
Sedatives and hypnotics causing adverse effects in therapeutic use
SEDATIVES HYPNOTICS
Sedatives/ Hypnotics
SEDATIVES/HYPNOTICS,OTHER
SEDATIVES/HYPONTICS
sedatol
Sedatuss DM Sirop
SEDC
sedcard
Seddera
Seddera arabica
Seddera hirsuta
Sedecal D
sedecamycin
sedecimal
Sedelia-Stress Tablets
sedentarily
sedentariness
Sedentary
Sedentary Exercise
sedentary life style
Sedentary lifestyle
Sedentary Lifestyles
sedentary work
Sedermyl
Sedes A
sedge
sedge family
Sedge Warbler
Sedge Warbler (Acrocephalus schoenobaenus)
Sedge Wren
Sedge, Flat
Sedge, Nut
Sedge, Sweet
sedges
Sedges, Flat
Sedges, Nut
Sedges, Sweet
sedi-stain
Sedicepan
sedieren
sedifluction
Sedilor
SEDIMENDATION RATE ERYTHROCYTES DECREASED
SEDIMENDATION RATE ERYTHROCYTES INCREASED
Sediment
sediment bacterium 15-27
sediment bacterium 15-31
sediment bacterium 15-39
sediment bacterium 15-41
sediment bacterium 22-39
sediment bacterium 23-01
sediment bacterium 23-02
sediment balance
sediment budget model
sediment content
sediment density
sediment discharge
sediment distribution
Sediment Filter
Sediment Filter Device Component
SEDIMENT GEOL
sediment layer
sediment layers
sediment petrography
Sediment Precipitate or Deposit in Medical Device or Device Ingredient
sediment sample
sediment samples
sediment sampling
sediment sump (of a well)
sediment transport
Sediment, Geologic
Sediment, Marine
Sediment, precipitate or deposit in device or device ingredient
sedimentary
sedimentary basin
sedimentary basins
sedimentary cycle
sedimentary deposition
sedimentary gneiss
sedimentary klippe
sedimentary rock
sedimentary rocks
Sedimentation
sedimentation basin
sedimentation basins
sedimentation coefficient
sedimentation constant
sedimentation equilibrium
Sedimentation Field Flow Fractionation
Sedimentation Field-Flow Fractionation
Sedimentation procedure
Sedimentation process
Sedimentation Rate Calculators
SEDIMENTATION RATE DECREASED
SEDIMENTATION RATE INCREASED
Sedimentation rate methods
Sedimentation Rate Units
Sedimentation Rate, Erythrocyte
Sedimentation Rates, Erythrocyte
sedimentation tank
sedimentation tanks
sedimentation velocity
Sedimentation, Blood
Sedimentation, Erythrocyte
sedimented
Sedimentibacter
Sedimentibacter Breitenstein et al. 2002
Sedimentibacter hongkongensis
Sedimentibacter hydroxybenzoicus
Sedimentibacter hydroxybenzoicus (Zhang et al. 1994) Breitenstein et al. 2002
Sedimentibacter saalensis
Sedimentibacter saalensis Breitenstein et al. 2002
Sedimentibacter sp. B4
Sedimentibacter sp. BAF1
Sedimentibacter sp. BD7-4
Sedimentibacter sp. BRS2
Sedimentibacter sp. C7
Sedimentibacter sp. D7
Sedimentibacter sp. IMPC3
Sedimentibacter sp. JN18_A14_H
Sedimentibacter sp. JN18_V27_I
Sedimenticola
Sedimenticola Narasingarao and Haggblom 2006
Sedimenticola selenatireducens
Sedimenticola selenatireducens Narasingarao and Haggblom 2006
sedimenting
sedimentite
sedimentological
sedimentology
Sedimentometers
sediments
SEDIMENTS GEOL
Sediments, Geologic
Sediments, Marine
Sediminibacillus
Sediminibacillus halophilus
Sediminibacillus sp. GDS1-2
Sediminibacillus sp. GDS1-3
Sediminibacter
Sediminibacter furfurosus
Sediminibacter furfurosus Khan et al. 2007
Sediminibacter Khan et al. 2007
Sediminibacter sp. KYW39
Sediminibacterium
Sediminibacterium ginsengisoli
Sediminibacterium Qu and Yuan 2008
Sediminibacterium salmoneum
Sediminibacterium salmoneum Qu and Yuan 2008
Sediminibacterium sp. I-28
Sediminibacterium sp. I-32
Sediminibacterium sp. IV-105
Sediminibacterium sp. IV-28
Sediminibacterium sp. IV-37
Sediminibacterium sp. TEGAF015
Sediminicola
Sediminicola Khan et al. 2006
Sediminicola luteus
Sediminicola luteus Khan et al. 2006
Sediminitomix
Sediminitomix flava
Sediminitomix flava Khan et al. 2007
Sediminitomix Khan et al. 2007
Sedirea
Sedirea japonica
Sedirea japonica (L.Linden et Rchb.f.) Garay et H.R.Sweet
sedis Fungi, incertae
sedis Fungus, incertae
Sedistal
sedition
seditionaries
seditionary
seditionous
seditionously
seditious
seditiously
Sedivet
SEDK
SEDL
SEDL Gene Mutation Detection Reagents
SEDL protein, human
SEDL protein, mouse
SEDL, 1-BP DEL, 613A
SEDL, 2-BP DEL, 157AT
SEDL, 2-BP DEL, 191TG
SEDL, 2-BP DEL, 53TT
SEDL, 5-BP DEL, NT267
SEDL, 5-BP DEL, NT271
SEDL, IVS3DS, G-A, +5
SEDL, IVS4, T-C, +4
SEDL, LEU131TER
SEDL, PHE83SER
SEDL, SER110TER
Sedlackova syndrome
SEDLIN
sedlin protein, human
sedlin protein, mouse
SEDLP1
Sedocalaine
Sedoheptitol
Sedoheptitol | Urine
Sedoheptitol/creat Ur-sRto
Sedoheptitol/Creatinine
Sedoheptitol/Creatinine [Molar ratio] in Urine
Sedoheptitol/Creatinine:ScRto:Pt:Urine:Qn
Sedoheptitol/Creatinine:Substance Concentration Ratio:Point in time:Urine:Quantitative
Sedoheptulokinase
sedoheptulokinase (phosphorylating)
sedoheptulokinase activity
sedoheptulokinase, human
sedoheptulokinase, mouse
sedoheptulose
sedoheptulose 1,7-bisphosphatase activity
sedoheptulose 1,7-bisphosphate
sedoheptulose 1,7-diphosphatase activity
sedoheptulose 1,7-diphosphate phosphatase
sedoheptulose 1,7-diphosphate phosphatase activity
sedoheptulose 7-phosphate
sedoheptulose bisphosphatase activity
sedoheptulose diphosphatase
sedoheptulose diphosphatase activity
sedoheptulose-1,7-biphosphatase
sedoheptulose-1,7-bisphosphatase activity
sedoheptulose-1,7-bisphosphate 1-phosphohydrolase activity
Sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate glyceronetransferase
sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate glyceronetransferase activity
Sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate glycolaldehydetransferase
sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate glycolaldehydetransferase activity
sedoheptulose-bisphosphatase
sedoheptulose-bisphosphatase activity
sedoheptulose, 1,3-di-(13)O-labeled
sedolisin
Sedormid
Sedotime
Sedoval
Sedoval K-17
sedoxantrone trihydrochloride
SEDP cpd
sedridine
sedridine, (S-(R*,S*))-isomer
SEDT
SEDT WITH MENTAL RETARDATION
SEDT-PA
seduce
seduced
seducement
seducements
seducer
seducers
seduces
seducest
seduceth
seducible
seducing
seduction
seductions
seductive
seductively
seductress
seductresses
sedulity
sedulous
sedulously
sedulousness
Sedum
Sedum acre
Sedum aizoon
Sedum alboroseum
Sedum alboroseum Baker
Sedum album
Sedum alexanderi
Sedum alexanderi Eggli
Sedum alfredii
Sedum alfredii Hance
Sedum algidum
Sedum allantoides
Sedum amabilis
Sedum anacampseros
Sedum bergeri
Sedum bulbiferum
Sedum bupleuroides
Sedum burrito
Sedum caeruleum
Sedum calvatum
Sedum chrysanthemifoliim
Sedum clavatum
Sedum commixtum
Sedum compactum
Sedum corynephyllum
Sedum cretinii
Sedum dasyphyllum
Sedum dumulosum
Sedum farinosum
Sedum fastigiatum
Sedum furfuraceum
Sedum fusiforme
Sedum gracile
Sedum hakonense
Sedum hemsleyanum
Sedum heterodontum
Sedum himalensis
Sedum hispanicum
Sedum humifusum
Sedum humifusum Rose
Sedum humile
Sedum hybridum
Sedum hybridum L.
Sedum integrifolium
Sedum integrifolium (Raf.) A.Nelson
Sedum ishidae
Sedum jaccardianum
Sedum japonicum
Sedum kamtschaticum
Sedum kirilowii
Sedum laconicum
Sedum lanceolatum
Sedum lancerotense
Sedum latent virus
Sedum lineare
Sedum lydium
Sedum macrocarpum
Sedum magellense
Sedum makinoi
Sedum mexicanum
Sedum meyeri-johannis
Sedum modestum
Sedum morrisonense
Sedum multicaule
Sedum multiceps
Sedum nepalicum
Sedum nobilis
Sedum nudum
Sedum oaxacanum
Sedum obcordatum
Sedum obtusatum
Sedum oreades
Sedum oryzifolium
Sedum palmeri
Sedum platyphyllum Alexander
Sedum praealtum
Sedum praealtums
Sedum pubescens
Sedum purpureoviride
Sedum rhodanthum
Sedum rhodanthum A.Gray
Sedum roseum
Sedum rubrotinctum
Sedum rupestre
Sedum sarmentosum
Sedum sediforme
Sedum selskianum
Sedum selskianum Regel et Maack
Sedum serratum
Sedum sexangulare
Sedum sexangulare L.
Sedum sikokianum
Sedum sinuatum
Sedum spectabile
Sedum spectabile Boreau
Sedum spurium
Sedum subtile
Sedum surculosum
Sedum telephium
Sedum telephium subsp. alboroseum
Sedum telephium subsp. alboroseum (Baker) Froed.
Sedum ternatum
Sedum tosaense
Sedum triactina
Sedum trullipetalum
Sedum urvillei
Sedum wallichianum
Sedum yabeanum
Sedum yunnanense
Sedum zentaro-tashiroi
Sedums
Seduxen
Sedyn-A-forte
See
See ({277600}) for a phenotypically similar autosomal recessive form
See ({608328}) for a phenotypically similar autosomal dominant form
See {177850} for description of heterozygous phenotype
See {255160} for an autosomal recessive form
See {607731} for an autosomal recessive form
See {608590} for an autosomal dominant form
see above
see again
See AI1B ({104500}) for an allelic autosomal dominant form
see also
See also {606190})
See also a childhood-onset form ({114100})
See also adult-onset stiff person syndrome ({184850})
See also an adult-onset form ({213600})
See also antenatal Bartter syndrome type 1 ({601678}) and Bartter syndrome type 2 ({241200})
See also Antley-Bixler syndrome (ABS) with normal steroidogenesis ({207410})
See also autosomal dominant FMF ({134610}), caused by heterozygous mutations in the MEFV gene
See also autosomal dominant form ({128230})
See also autosomal dominant form ({160800}), which is less common and less severe
See also autosomal dominant form ({176860})
See also autosomal dominant giant axonal neuropathy ({610100})
See also autosomal dominant hypophosphatemic rickets ({193100})
See also autosomal dominant PEOA1 ({157640})
See also autosomal dominant sick sinus syndrome ({163800})
See also autosomal recessive familial Mediterranean fever (FMF, {249100})
See also autosomal recessive form ({255700}), which is more common and more severe
See also autosomal recessive form ({612304})
See also autosomal recessive giant axonal neuropathy ({256850})
See also autosomal recessive limb-girdle muscular dystrophy 2K with mental retardation (LGMD2K, {609308}), an allelic disorder with a milder phenotype and no cortical structural abnormalities
See also autosomal recessive PEOB ({258450)}
See also autosomal recessive sick sinus syndrome (SSS1, {608567})
See also benign familial infantile convulsions (BFIC1, {601764})
See also benign familial neonatal-infantile convulsions (BFNIS, {607745}), which shows some phenotypic similarities
See also benign neonatal epilepsy (EBN1, {121200})
See also CblC ({277400})
See also CblD ({277410})
See also CMTX1 ({302800}) and CMT3X ({302802})
See also CMTX1 ({302800}) and CMTX2 ({302801})
See also congenital stiff person syndrome ({149400})
See also Crigler-Najjar syndrome type I ({218800}) which is also due to mutations in UGT1 ({191740})
See also cytochrome b-positive autosomal recessive CGD ({233700} and {233710})
See also DA2B ({601680}), which is an allelic disorder
See also Dent disease 2 ({300555})
See also distal HMN2A ({158590})
See also dominant DEB ({131750}), an allelic disorder with a less severe phenotype
See also dominant DEB ({131750}), an allelic disorder with a similar phenotype
See also Dyggve-Melchior-Clausen disease ({223800})
See also dyssegmental dysplasia, Silverman-Handmaker type ({224410})
See also ECYT2 ({263400}) and ECYT3 ({609820})
See also EIEE1 ({308350})
See also erythrocytosis 1 (ECYT1, {133100})
See also facial hemihypertrophy ({133900})
See also familial cold inflammatory syndrome ({120100}), an allelic disorder with overlapping features
See also familial developmental dysphasia ({600117})
See also febrile seizures (FEB1, {121210})
See also French-Canadian type of Leigh syndrome ({220111})
See also Gaucher disease type III ({231000}), which is much less severe
See also Glanzmann thrombasthenia due to mutations in integrin alpha 2B ({273800})
See also Griscelli syndrome type 1 ({214450}) for a similar disorder without immunological abnormalities and Griscelli syndrome type 3 ({609227}) for a similar disorder without neurologic or immunologic abnormalities
See also Griscelli syndrome type 2 ({607624}) for a similar disorder with characteristic immunologic abnormalities and Griscelli syndrome type 3 ({609227}) for a similar disorder without neurologic or immunologic abnormalities
See also Griscelli syndrome, type 1 ({214450}) for a similar disorder with characteristic neurologic disease and Griscelli syndrome, type 2 ({607624}) for a similar disorder with characteristic immunodeficiency/hemophagocytic syndrome.
See also hepatocerebral form of mtDNA depletion ({251880})
See also hereditary hemorrhagic telangiectasia (HHT)-related pulmonary artery hypertension (HHT2, {600376})
See also HMN2B ({608634})
See also infantile ({600649}) and late-onset ({255110}) CPT II deficiency
See also isolated pneumothorax ({173600}), an allelic disorder that may represent a mild form of the BHD syndrome
See also junctional EB with pyloric atresia ({226730})
See also later childhood-onset form ({300718})
See also Leigh syndrome ({256000})
See also lethal neonatal ({608836}) and adult forms ({255110})
See also MMAA ({251100})
See also MMAB ({251110})
See also MNGIE ({603041}), a similar disorder with overlapping clinical features
See also more severe phenotype peeling skin syndrome ({270300})
See also Muckle-Wells syndrome ({191900}), an allelic disorder with overlapping features
See also OCA1B, or 'yellow albinism,' an allelic disorder with residual tyrosinase activity and some pigmentation
See also optic atrophy 1 ({165500}), an allelic disorder without deafness
See also optic atrophy with deafness ({125250}), an allelic disorder
See also pachyonychia congenita, type 3 (PC1, {167200})
See also PARK6 ({605909}), PARK7 ({606324}), and PARK9 ({606693}) for autosomal recessive disorders with overlapping phenotypes
See also peeling skin syndrome, acral type ({609796})
See also perinatal lethal variant ({608013}), which is more severe
See also PFM3 on chromosome 4q21-q23 ({609566})
See also PGL1 ({168000})
See also PGL2 ({601650}), PGL3 ({605373}), and PGL4 ({115310})
See also pseudohypoparathyroidism type Ia ({103580})
See also pseudohypoparathyroidism type Ib ({603233}) and Ic ({612462})
See also pseudopseudohypoparathyroidism ({612463})
See also recessive DEB ({226600}), an allelic disorder with a more severe phenotype
See also renal-hepatic-pancreatic dysplasia ({208540})
See also severe, early-onset form ({300717})
See also simplex EB with pyloric atresia ({612138})
See also Simpson-Golabi-Behmel syndrome 1 (SGBS1, {312870})
See also the homozygous state, mosaic variegated aneuploidy (MVA, {257300})
See also the lethal neonatal ({608836}) and infantile ({600649}) forms
See also the myopathic form of the disorder ({609560})
See also the non-Herlitz type of JEB ({226650}), a less severe disorder
See also the X-linked form ({300291})
See also X-linked ({310400}) and autosomal dominant ({160150}) forms
See also X-linked ({310400}) and autosomal recessive ({255200}) forms
See also X-linked alpha-thalassemia/mental retardation syndrome ({301040})
See also X-linked dominant form ({300652})
See also X-linked EDMD ({310300})
See also X-linked Leigh syndrome ({308930})
See also X-linked nephrocalcinosis ({310468}), X-linked recessive hypophosphatemic rickets ({300554}), and low-molecular-weight proteinuria with nephrocalcinosis ({308990})
see below
see chapter 3
see chapter 3 - Ethnic Group
see chapter 3 - Race
see clearly
See CMT4A ({214400}) for autosomal recessive demyelinating forms
see description
See EBN1 ({121200}) for an autosomal dominant form
see endorsement
See entry {104300} for general information on Alzheimer disease
see figures 1 to 5
See Joubert syndrome 7 ({611560}), an allelic disorder with a less severe phenotype
See juvenile myoclonic epilepsy ({606904})
see me tomorrow
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