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235 Cards in this Set
- Front
- Back
5 layers of epidermis from outside -> in
|
stratum Corneum
s. Lucidum s. Granulosum s. Spinosum s. Basalis (Californians Like Girls in String Bikinis) |
|
3 kinds of epithelial cell junctions
|
tight
anchoring gap |
|
tight junctions are aka ___
they connect a cell to ___ they are located at ___ and do ___ (2) |
zona occludens
another cell apical end of cell maintain epithelial polarization prevent paracellular leakage |
|
2 proteins which make up tight junction
|
claudin
occludin |
|
4 kinds of anchoring junctions
|
adherens junction
desmosomes focal adhesions hemidesmosomes |
|
adherens junctions are aka ___ (2)
they connect a cell to ___ they are located at ___ |
zona adherens
intermediate junctions another cell apex beneath tight junction |
|
adherens junctions use ___ to connect to ___
|
cadherins
actin cytoskeleton |
|
cadherins require ___ to work
|
Ca2+
|
|
desmosomes are aka ___
they connect a cell to ___ they are located ___ |
macula adherens
another cell sporadically |
|
desmosomes use ___ to connect to ___
|
cadherins
intermediate filament cytoskeleton (e.g. keratin) |
|
focal adhesions connect a cell to ___
they connect the membrane to ___ |
ECM
actin cytoskeleton |
|
hemidesmosomes connect a cell to ___
they connect the membrane to ___ |
ECM
intermediate filament cytoskeleton |
|
in desmosomes, ____ is an intracellular protein which binds ___,
which does extracellular adhesion, and ___ |
desmoplakin
cadherin intermediate filaments |
|
unhappy knee triad
|
medial collateral ligament
anterior cruciate l. lateral meniscus |
|
unhappy triad is caused by blow from the ___ side
|
lateral
|
|
___ indicates torn ACL
|
anterior drawer sign (tibia moves too far forward)
|
|
___ indicates torn PCL
|
posterior drawer sign (tibia moves too far backward)
|
|
___ indicates torn MCL
|
abnormal passive abduction
|
|
rotator cuff muscles
(in CW order of insertions on R humerus when viewed laterally, starting at 12) |
supraspinatus
subscapularis teres minor infraspinatus |
|
supraspinatus does ___ to humerus
|
abduction
|
|
subscapularis does ___ to humerus (2)
|
internal rotation
adduction |
|
teres minor does ___ to humerus (2)
|
external rotation
adduction |
|
infraspinatus does ___ to humerus
|
external rotation
|
|
3 dermatomes of medial arm/forearm/hand,
from proximal to distal |
T2
T1 C8 |
|
4 dermatomes of lateral arm/forearm/hand,
from proximal to distal |
C4 (shoulder)
C5 (upper arm) C6 (forearm + lateral 2 digits) C7 (middle wrist + 3rd digit) |
|
C6 has finger(s)
|
1
2 |
|
C7 has finger(s)
|
3
|
|
C8 has finger(s)
|
4
5 |
|
Erb's palsy is from ___ lesion
2 causes are ___ it pw ___ |
superior brachial plexus trunk (C5 + C6 roots)
shoulder dystocia trauma waiter's tip |
|
waiter's tip posture includes ___ (3)
|
adduction of humerus
medial rotation of humerus elbow pronation |
|
Klumpke's palsy is from ___ lesion
4 causes are ___ it pw ___ |
inferior brachial plexus trunk (C8 + T1 roots)
congenital defect shoulder dystocia traction from hanging by one arm compression by cervical rib thoracic outlet syndrome Pancoast tumor |
|
thoracic outlet syndrome includes ___ (5)
|
thenar + hypothenar atrophy
lumbricals + interossei atrophy medial hand + forearm sensory deficit radial pulse absent on rotating head ipsilateral to lesion Horner's syndrome |
|
loss of lumbricals + interossei in Klumpke's palsy causes ___
|
total claw hand
|
|
lumbricals are innervated by ___ fibers of ___ (2) n.s
they do ___ (3) |
C8 + T1
median (1st + 2nd) ulnar (3rd + 4th) MCP flexion PIP extension DIP extension |
|
interossei are innervated by ___ fibers of ___ n.
they do ___ (2) |
C8 + T1
ulnar abduction (dorsal interossei) adduction (volar interossei) |
|
thumb opposition is done by ___ branch of ___ n.
it can be injured by ___ muscle is ___ |
recurrent
median superficial laceration opponens pollicis |
|
saturday night palsy is injury of ___
it causes ___ (4) motor deficits and ___ (3) sensory deficits |
radial n.
wrist drop (wrist extensor palsy) finger extensor palsy thumb abduction palsy supinator palsy posterior arm posterior hand dorsal thumb |
|
proximal median n. lesion is caused by ___
it causes ___ motor deficit and ___ (2) sensory deficits |
supracondylar humerus fx
thumb opposition ("ape hand") lateral 3.5 fingers (dorsal and volar) thenar eminence |
|
distal median n. lesion is caused by ___ (2)
it causes ___ motor deficit and ___ sensory deficit |
carpal tunnel syndrome
lunate dislocation lateral finger flexion palsy (lumbricals) lateral 3.5 fingers (dorsal and volar) |
|
sign of distal median n. lesion
|
ulnar deviation with wrist flexion
|
|
proximal ulnar n. lesion is caused by ___
it causes ___ (2) motor deficits and ___ (2) sensory deficits |
medial epicondylar humerus fx
medial finger flexion palsy wrist flexion palsy medial 1.5 fingers hypothenar eminence |
|
sign of proximal ulnar n. leison
|
radial deviation with wrist flexion
|
|
distal ulnar n. lesion is caused by ___
it causes ___ (3) motor deficits and ___ (2) sensory deficit |
hook of hamate fx
interossei palsy adductor pollicis palsy medial lumbricals palsy medial 1.5 fingers hypothenar eminence |
|
sign of distal ulnar n. lesion
|
ulnar claw hand
|
|
ulnar claw hand means ___
|
pope's benediction sign when asked to extend all fingers
|
|
the posterior interosseus is a branch of ___ n.
it may be injured by ___ it is a continuation of ___ after the latter does ___ it innervates ___ |
radial
radial subluxation deep branch of radial gives branches to supinator and ECRB hand extensors |
|
midshaft fx of humerus injures ___ n. in ___
|
radial
spiral groove |
|
tennis elbow is ___
golf elbow is ___ |
lateral epicondylitis
medial epicondylitis |
|
anterior interosseus n. is a branch of ___ n.
it innervates ___ (3) |
median
flexor pollicis longus pronator quadratus flexor digitorum profundus (lateral 2 digits) |
|
4 muscles innervated by radial n.
|
Brachioradialis
Extensors of wrist + fingers Supinator Triceps |
|
obturator n. lesions are caused by ___
they cause motor deficit for ___ and sensory deficit for ___ |
anterior hip dislocation
thigh adduction medial thigh |
|
femoral n. lesions are caused by ___
they cause motor deficit for ___ (2) and sensory deficit for ___ (2) |
pelvic fx
hip flexion knee extension anterior thigh medial leg |
|
common peroneal n. lesions are caused by ___ (2)
they cause motor deficit for ___ (3) and sensory deficit for ___ (2) |
fibular neck fx
lateral leg trauma foot eversion foot dorsiflexion toe extension anterolateral leg dorsal foot |
|
tibial n. lesions are caused by ___
they cause motor deficit for ___ (3) and sensory deficit for ___ |
knee trauma
foot inversion foot plantarflexion toe flexion sole of foot |
|
superior gluteal n. lesions are caused by ___ (2)
they cause motor deficit for ___ and sensory deficit for ___ |
posterior hip dislocation
polio thigh abduction none |
|
thigh abduction deficit in sup. gluteal n. palsy is called ___
|
Trendelenburg sign
|
|
inferior gluteal n. lesions are caused by ___
they cause motor deficit for ___ and sensory deficit for ___ |
posterior hip dislocation
hip extension (jumping, stair climbing, getting up from chair) none |
|
in sarcomere, 2 thick bands and intervening white space define ___
|
A band
|
|
___ is the white zone in the middle of the A band
___ is the line in the middle of that zone |
H band
M line |
|
___s extend from M line
|
myosin fibers
|
|
adjacent A bands are separated by ___
|
I bands
|
|
___ is the line in the middle of the I band
|
Z line
|
|
___s extend from Z line
|
actin fibers
|
|
on contraction, ____ bands shrink
|
H
I |
|
in skeletal muscle, depolarization of ___ (2) in muscle causes ___ current through ___ receptors
this causes ___ current through ___ receptors in ___ |
plasma membrane
t-tubules Ca2+ DHP Ca2+ ryanodine sarcoplasmic reticulum |
|
DHP channels are aka ___
|
L type
|
|
type ___ fibers are slow twitch
they are ___ colored they have ___ metabolism |
I
red aerobic |
|
4 steps in myosin power stroke
|
ATP binding/ADP release
cocking cross-bridging power stroke |
|
reaction in cocking step of power stroke
|
ATP hydrolysis
|
|
reaction in cross-bridging step of power stroke
|
Ca2+ binding TnC
|
|
reaction in power stroke step of power stroke
|
P_i release
|
|
2 kinds of bone formation
|
endochondral
membranous |
|
endochondral bone growth is for ___ bones
membranous is for ___ |
longitudinal
flat |
|
___ bone growth happens in 3 steps
the first is ___ the second is ___ the third is ___ |
endochondral
cartilaginous model replacement of model with woven bone lamellar bone |
|
cartilaginous model for endochondral ossification is made by ___
woven bone replacement is made by ___ (2) |
chondrocytes
osteoblasts osteoclasts |
|
osteoblast stem cells live in ___
they are from ___ lineage |
periosteum
mesenchyme |
|
membranous ossification happens in ___ steps
these are ___ |
2
woven bone lamellar bone |
|
achondroplasia is a defect in ___ ossification
|
endochondral
|
|
T/F: achondroplasia is usually inherited
|
false (85% sporadic)
|
|
2 kinds of osteoporosis
|
post-menopausal
senile (after 70 y.o.) |
|
Ca2+ prophylaxis for osteoporosis begins before age ___
|
30
|
|
osteopetrosis is deficiency of ___
|
bone resorption
|
|
bone resorption defect in osteopetrosis is due to ___
defective enzyme is ___ |
defective osteoclasts
carbonic anhydrase II |
|
blood chemistry in osteopetrosis is normal/abnormal
|
normal
|
|
CBC in osteopetrosis is normal/abnormal
|
abnormal
|
|
3 CBC abnormalities in osteopetrosis
|
anemia
leukopenia thrombocytopenia (reduced bone marrow space) |
|
X-ray finding in osteopetrosis
|
erlenmeyer flask bones
|
|
neurological problem in osteopetrosis
this is caused by ___ |
CN impingement
narrowing foramina |
|
3 abormal blood levels in osteomalacia
|
high PTH
low Ca2+ low phosphate |
|
___ is bone defect caused by hyper PTH
|
osteitis fibrosa cystica
|
|
osteitis fibrosa cystica has normal/abnormal blood chemistry
|
abnormal
|
|
gross histopath in osteitis fibrosa cystica
|
brown tumor
|
|
brown tumor of osteitis fibrosa cystica is lined by ___
|
osteoclasts
|
|
3 lab findings in osteitis fibrosa cystica
|
high Ca2+
low phosphate high ALP |
|
Paget's disease of bone is aka ___
it is caused by ___ |
osteitis deformans
increased osteoblast + osteoclast activity |
|
lab finding in Paget's disease of bone
|
high ALP
|
|
in ___ bone is replaced by fibroblasts and ___ (2)
___ is one subtype with unilateral lesions and endocrine abnormalities |
polyostotic fibrous dysplasia
collagen irregular trabeculae McCune Albright |
|
main endocrine abnormality in McCune Albright
|
precocious puberty
|
|
skin finding in McCune Albright
|
cafe au lait spots
|
|
___ aka ___ is most common benign bone tumor
|
osteochondroma
exostosis |
|
osteochondroma has ___ bone with ___
typically occurs in ___ population typically occurs in ___ in body |
mature
cartilaginous cap men<25 y.o. long bone metaphysis |
|
osteochondroma ___ly transforms to osteosarcoma
|
infrequently
|
|
enchondroma is located in ___ of bone
and ___ of body |
intramedullary
distal extremity |
|
giant cell tumor aka ___ has peak incidence at ___ y.o.
sign on X-ray is ___ or ___ typically occurs in ___ or ___ |
osteoclastoma
20--40 double bubble soap bubble distal femur proximal tibia |
|
osteoma is associated with ___ syndrome
commonly occurs in ___ |
Gardner's
skull |
|
osteoid osteoma and ____ have interlacing trabeculae of ___
surrounded by ___ |
osteoblastoma
woven bone osteoblasts |
|
osteoid ostseoma size is ___
it is located in ___ and ___ |
<2 cm
proximal femur proximal tibia |
|
osteoblastoma size is ___
it is located in ___ |
>2 cm
vertebral column |
|
most common 1' malignancy of bone
|
multiple myeloma
|
|
___ aka ___ is 2nd most common 1' malignancy of bone
|
osteosarcoma
osteogenic sarcoma |
|
osteosarcoma has peak incidence in ___
|
men 10--20 y.o
|
|
osteosarcoma occurs in ___ of ___ bones
usually in ___ or ___ in body 2 signs on X-ray are ___ |
metaphysis
long distal femur proximal tibia Codman's triangle sunburst pattern |
|
Codman's triangle indicates ___
|
periosteal elevation
|
|
4 osteosarcoma RFs
|
Paget's disease of bone
bone infarct radiation familial retinoblastoma |
|
Ewing sarcoma occurs in ___ of ___ (4) bones
|
diaphysis
long bones pelvis scapula ribs |
|
microscopic histopath of Ewing's sa has ___ (2)
|
small blue cells
onion skin appearance |
|
translocation in Ewing's sa
|
11;22
|
|
peak incidence for Ewing's sa
|
boys <15 y.o.
|
|
chondrosarcoma is most commonly in ___ (6) bones
|
humerus
scapula spine pelvis femur tibia |
|
peak incidence for chondrosarcoma
|
men 30--60
|
|
gross histopath for chondrosa
|
glistening mass in medullary cavity
|
|
2 knuckle deformities in osteoarthritis
|
Bouchard's nodes
Heberden's nodes |
|
Bouchard's nodes occur at ___ joint
|
PIP
|
|
osteoarthritis is worse at ___ time of day
|
end of day (after use)
|
|
knee osteoarthritis starts in ___ aspect
|
medial
|
|
RA is a type ___ hypersensitivity
it affects men/women more it is linked to gene ___ |
3
women HLA-DR4 |
|
2 serum abnormalities for RA
___ is more sensitive ___ is more specific |
rheumatoid factor
anti-CCP rheumatoid factor anti-CCP |
|
anti-CCP Abs attack ___ (3)
|
filaggrin
vimentin keratin |
|
2 findings in Sjögren syndrome
|
enlarged parotid
dental caries |
|
Sjögren syndrome has increased risk of ___ (2)
|
B cell Ly
dental caries |
|
2 serum findings in Sjögren syndrome
___ is more specific |
anti SS-A (Ro)
anti SS-B (La) anti SS-B (La) |
|
Sjögren syndrome has peak incidence in ___
|
women 40--60 y.o.
|
|
gouty tophus is made from ___ located in ___
|
uric acid
fibrous tissue |
|
gout attacks follow ___ (2)
|
large meal
alcohol consumption |
|
alcohol intake causes gout attack because
|
metabolites compete in kidney with uric acid for excretion
|
|
glycogen storage disease associated with gout
|
Von Gierke
|
|
___% of gout is due to urate overproduction
the rest is due to ___ |
10
underexcretion |
|
diuretics which cause underexcretion
|
thiazides
|
|
urate crystals are ___ shaped
they are ___ly birefringent this means they are ___ colored when aligned ___ to light |
needle
negatively yellow parallel |
|
gout is more common in men/women
|
men
|
|
4 drugs for gout
___ (2) can be used for acute attack |
NSAIDs
colchicine allopurinol probenecid NSAIDs colchicine |
|
preferred NSAID for gout
|
indomethacin
|
|
avoid ___ drugs in gout, because ___
|
salicylate
they depress urate excretion (in low doses) |
|
colchicine prevents ___ (2) by ___ing, which does ___
|
leukocyte degranulation
leukocyte chemotaxis binding tubulin monomers prevents microtubule polymerization |
|
probenecid does ___
|
increases urate excretion in PCT
|
|
probenecid interacts with other drugs by ___ing
|
preventing their excretion
|
|
allopurinol works by ___ing
|
inhibiting xanthine oxidase
|
|
xanthine oxidase does ___ (2)
|
hypoxanthine -> xanthine
xanthine -> uric acid |
|
allopurinol interacts with ___ (2) drugs by ___ing
|
azathioprine
6-MP preventing their breakdown by xanthine oxidase |
|
pseudogout crystals are made of ___
they are ___ shaped they are ___ly birefringent |
Ca2+ pyrophosphate
rhomboid positively |
|
pseudogout mainly affects men/women
|
both equally
|
|
joint most commonly affected in pseudogout
|
knee
|
|
tx for pseudogout
|
none!
|
|
2 non-spinal sx of ankylosing spondylitis
|
uveitis
aortic regurg |
|
psoriatic arthritis happens in ___% of psoriasis
it pw ___ and ___ on X-ray |
33
dactylitis (sausage finger) pencil-in-cup deformity |
|
3 serum findings in SLE
1 serum finding in drug-induced SLE |
ANA
anti-dsDNA anti-Smith anti-histone |
|
SLE marker ___ is specific but not prognostic
SLE marker ___ is specific with poor prognosis |
anti-Smith
anti-dsDNA |
|
SLE marker ___ is sensitive but not specific
|
ANA
|
|
3 abnormal lab values in sarcoidosis
|
vitamin D
Ca2+ ACE |
|
inflammation associated with sarcoidosis
|
uveoparotitis
|
|
3 micro histopath findings in sarcoidosis
|
noncaseating granulomas
Schaumann bodies asteroid bodies |
|
Schaumann bodies are ___
|
calcifications inside giant cell
|
|
polymyalgia rheumatica causes pain in ___ (2)
it is associated with ___ |
shoulders
hips GCA |
|
polymylagia rheumatica has high ___ and normal ___
|
ESR
CPK |
|
tx for polymyalgia rheumatica
|
CS
|
|
polymyositis is caused by ___
it usually affects ___ in body dx is via ___ |
CD8 attack on muscle fibers
shoulders bx |
|
dermatomyositis has features of ___
plus ___ (3) |
polymyositis
heliotrope rash Gottron's papules increased risk of malignancy |
|
Gottron's papules are ___
|
pink patches on extensor surfaces + knuckles
|
|
4 lab findings in polymyositis/dermatomyositis
|
CPK
aldolase ANA anti-Jo-1 |
|
tx for polymyositis/dermatomyositis
|
CS
|
|
mixed connective tissue disease pw ___ (5)
|
Raynaud's phenomenon
Fatigue Arthralgia Myalgia Esophageal dysmotility |
|
serum finding in mixed connective tissue disease
|
anti-U1RNP
|
|
2 kinds of scleroderma
___ is worse |
diffuse scleroderma
CREST syndrome diffuse scleroderma |
|
serum finding in diffuse scleroderma
|
anti-Scl-70
|
|
Scl-70 is aka ___
|
topoisomerase I
|
|
serum finding in CREST syndrome
|
anti-centromere
|
|
rhabdomyoma of ___ is associated with the phakomatosis ___
|
heart
tuberous sclerosis |
|
2 histopath changes in psoriasis
|
hyperkeratosis
parakeratosis |
|
hyperkeratosis means ___
|
thickened stratum corneum
|
|
parakeratosis means ___
|
nuclei retained in stratum corneum
|
|
in psoriasis,
s. granulosum is ___ s. spinosum is ___ |
thin
thick |
|
finding on fingers in psoriasis
|
nail pitting
|
|
suborrheic keratosis has ___-filled cysts
sudden appearance of multiple keratoses can mean ___ |
keratin
cancer (GI, Ly) |
|
cellulitis is usually caused by ___ (2)
|
SA
S. pyogenes |
|
necrotizing fasciitis is caused by ___ (2)
|
S. pyogenes
anaerobes |
|
Staph scalded skin syndrome toxin affects ___ of skin
|
s. granulosum
|
|
hairy leukoplakia in HIV is caused by ___
|
EBV
|
|
pemphigus/pemphigoid is worse
|
pemphigus
|
|
histopath finding in pemphigus vulgaris
|
acantholysis (intraepidermal bullae) of skin + oral mucosa
|
|
IF finding in pemphigus vulgaris
|
netlike IgG pattern in epidemis
|
|
clinical sign in pemphigus vulgaris
|
separation of epidermis with stroking (Nikolsky's sign)
|
|
Abs in pemphigus vulgaris are against
|
desmosomes
|
|
bullous pemphigoid is similar to ___ but doesn't affect ___
Nikolsky's sign is ___ |
pemphigus vulgaris
oral mucosa negative |
|
IF pattern in bullous pemphigoid
|
linear IgG below epidermis
|
|
Abs in bullous pemphigoid are against ___
|
hemidesmosomes
|
|
bullous pemphigoid has ___ inside blisters
|
eosinophils
|
|
dermatitis herpetiformis is associated with ___
it pw ___ |
celiac
pruritic papules + vesicles |
|
immunohistopath finding in dermatitis herpetiformis
|
IgA at tips of dermal papillae
|
|
lichen planus pw ___
it is associated with ___ |
purple polygonal pruritic papules
HCV |
|
micro histopath of lichen planus has ___ infiltrate at ___
|
sawtooth lymphocytic
dermal-epidermal junction |
|
histopath of acanthosis nigricans
|
s. spinosum hyperplasia
|
|
erythema nodosum is associated with ___ (3)
|
granulomatous disease
streptococcal infection coccidioidomycosis |
|
5 granulomatous diseases associated with erythema nodosum
|
TB
leprosy sarcoidosis histoplasmosis Crohn's |
|
pityriasis rosea has ___ followed by ___ rash
it is not ___ |
herald patch
christmas tree (along rib line) infectious |
|
cherry hemangiomas appear at age ___
|
30--40
|
|
palisading nuclei occur in ___ skin cancer
|
BCC
|
|
arachidonic is released from ___ by ___
|
membrane lipids
PLA2 |
|
PLA2 is inhibited by ___
|
CS
|
|
2 kinds of enzyme which metabolize arachidonic acid
|
COX
lipooxygenase |
|
COX makes ___s
lipooxygenase makes ___s |
endoperoxides
hydroperoxides |
|
endoperoxides become ___ (3)
hydroperoxides become ___ |
PGs
PGI2 (prostacyclin) TX LTs |
|
LTB4 does ___
|
neutrophil chemotaxis
|
|
LTC4/D4/E4 does ___
|
bronchoconstriction
|
|
PGI2 does ___ (3)
|
reduced platelet aggregation
vasodilation reduced uterine tone |
|
PGE2 does ___ (4)
|
reduced vascular tone
pain increased uterine tone increased temperature |
|
TXA2 does ___ (2)
|
increased platelet aggregation
vasoconstriction |
|
zafirlukast does ___
|
LT R block
|
|
zileuton does ___
|
lipoxygenase inhibition
|
|
montelukast does ___
|
LT R block
|
|
low dose ASA is ___ and does ___
intermediate dose ASA is ___ and does ___ high dose ASA is ___ and does ___ |
<300 mg/d
platelet antiaggregant 300--2400 mg/d antipyretic + analgesic 2400--4000 mg/d anti-inflammatory |
|
3 SEs from chronic ASA
|
upper GI bleed
ARF interstitial nephritis |
|
COX1 is expressed in ___ cells
COX2 is expressed in ___ (2) cells |
most
inflammatory vascular endothelium |
|
platelets express COX___
|
1
|
|
___ is a COX2 selective inhibitor
|
celecoxib
|
|
2 SEs from celecoxib
|
thrombosis risk
sulfa allergy |
|
COX1 is important for ___ protection because ___
|
gastric
PGE1 inhibits H+ secretion |
|
acetaminophen is ___ (2) but isn't ___
|
antipyretic
analgesic anti-inflammatory |
|
bisphosphonates end in ___
they work by ___ing |
dronate
inducing osteoclast apoptosis |
|
bisphosphonates ___ hydroxyapatite formation and ___ hydroxyapatite resorption
|
reduce
reduce |
|
3 bisphosphonate indications
|
type I osteoporosis
hypercalcemia of malignancy Paget's disease of bone |
|
3 bisphosphonate SEs
|
corrosive esophagitis
nausea diarrhea |
|
3 kinds of biological anti-TNF drugs
___ is associated with TB reactivation |
etanercept
adalimumab infliximab infliximab |
|
etanercept is ___
it is indicated for ___ (3) |
soluble TNFR
RA psoriasis ankylosing spondylitis |
|
adalimumab is ___
it is indicated for ___ (3) |
anti TNFR mAb
RA psoriasis ankylosing spondylitis |
|
infliximab is ___
it is indicated for ___ (3) |
anti-TNF mAb
Crohn's RA ankylosing spondylitis |