Looking at these quiz slides from what appears to be a medical/biological sciences event in Gwalior, I can identify the questions being asked:
Q-1 (IMG_2089): "Link the images, identify the gentlemen who shared the 1984 Nobel Prize in Physiology or Medicine" - showing two men alongside a HAT medium selection diagram.
Q-2 (first image): "Identify the gentleman [who won the] Nobel Prize in Physiology or [Medicine]" - showing a black-and-white portrait.
Q-4 (third image): Another "link the images, identify gentlemen" question showing another portrait.
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1984 Nobel Prize Physiology Medicine HAT medium hybridoma monoclonal antibodies winners

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Nobel Prize Physiology Medicine HAT medium selection TK negative myeloma hybridoma

Here are the complete answers to all the quiz questions visible in your images:

Q-1 (IMG_2089) - 1984 Nobel Prize in Physiology or Medicine

The slide asks to link the two portraits with the HAT medium selection diagram.
The two gentlemen are Georges J.F. Köhler and César Milstein, who shared the 1984 Nobel Prize in Physiology or Medicine with Niels K. Jerne.
The HAT medium link: Köhler and Milstein developed hybridoma technology (1975) for producing monoclonal antibodies. The HAT (Hypoxanthine-Aminopterin-Thymidine) medium is the selection tool they used:
  • Myeloma cells (TK-) are HAT-sensitive - they die because aminopterin blocks the de novo DNA synthesis pathway, and they lack TK to use the salvage pathway
  • Splenic B-cells are mortal - they die on their own
  • Only the fused hybridoma cells (TK+) survive - they are immortal AND can use the salvage pathway
They were awarded "for the discovery of the principle for production of monoclonal antibodies."

Q-2 (First image) - Nobel Prize in Physiology or Medicine

The black-and-white portrait shown alongside the partially visible question asking to "Identify the gentleman [who won the] Nobel Prize in Physiology or [Medicine]" - given the context of the event (same series of questions on immunology/Nobel laureates), this is most likely Niels K. Jerne, the third co-laureate of the 1984 prize, who developed the clonal selection theory and network theory of the immune system.

Q-4 (Third image)

The blurry portrait on this slide appears to be part of the same "link the images" series (Q-4), likely showing another Nobel laureate in immunology or physiology - possibly César Milstein or another immunology pioneer, though the image is too blurry to confirm with certainty.

Summary table:
Prize YearLaureatesDiscovery
1984Niels K. JerneImmune network theory
1984Georges KöhlerMonoclonal antibody / hybridoma technology
1984César MilsteinMonoclonal antibody / hybridoma technology

CNS examination, Central nervous system examination.

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Now reading all major sections in parallel:
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Now reading the motor and sensory sections from Harrison's:
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I now have comprehensive content from Harrison's 22nd Edition. Let me compile the complete CNS examination guide.---

Complete CNS (Central Nervous System) Examination

Based on Harrison's Principles of Internal Medicine 22nd Ed. & Goldman-Cecil Medicine

OVERVIEW - ORDER OF EXAMINATION

A full CNS examination proceeds in this sequence:
  1. Higher Mental Functions (consciousness, cognition)
  2. Cranial Nerves (CN I-XII)
  3. Motor System (tone, power, reflexes, coordination)
  4. Sensory System (primary + cortical modalities)
  5. Gait & Cerebellar

PART 1: HIGHER MENTAL FUNCTIONS

Bare minimum: Level of consciousness + orientation to time, place, person.

A. Level of Consciousness

  • Ranges from fully awake to comatose
  • Describe the minimum stimulus needed to elicit a response:
    • Verbal commands
    • Squeeze of trapezius muscle (brief pain)
  • Distinguish purposeful responses (reaching toward pain, eye contact) from reflex spinal responses (triple flexion: ankle + knee + hip flexion to plantar stimulus)

B. Orientation

Ask the patient to state:
  • Name (person)
  • Location (place)
  • Day of week + date (time) - time is usually the first to be lost

C. Speech vs. Language

FeatureWhat to Assess
SpeechArticulation, rate, rhythm, prosody
LanguageVerbal/written output, response to commands, reading
Language testing sequence:
  1. Name components of a watch or pen (increasingly detailed)
  2. Repeat "No ifs, ands, or buts"
  3. Follow a 3-step verbal command
  4. Write a sentence
  5. Read and respond to a written command

D. Memory (3 Time Scales)

ScaleTest
ImmediateSay 3 items - patient repeats immediately
Short-termRecall same 3 items at 5 min and 15 min
Long-termPatient provides chronologic history of illness/personal events

E. Fund of Information

  • Ask about major historic or current events
  • Adjust for educational level and life experience

F. Insight & Judgment

  • Detected during interview
  • Formal test: "What would you do if you found a wallet on the sidewalk?"

G. Abstract Thought

  • Similarities: "How are an apple and an orange alike?"
  • List items with shared attributes: "Name four-legged animals"

H. Calculation

  • Age/education appropriate tasks
  • Serial 7s (subtract 7 from 100 repeatedly) or serial 3s from 20
  • Simple word problems

Cognitive Domains & Localization (Goldman-Cecil)

DomainLocalization
Memory (episodic)Medial temporal lobe (hippocampus)
LanguageLeft perisylvian cortex
Visuospatial cognitionParietal / right hemisphere
Executive functionPrefrontal cortex

PART 2: CRANIAL NERVE (CN) EXAMINATION

Bare minimum: Check fundi, visual fields, pupils (size & reactivity), extraocular movements, facial movements.
Test CNs in numerical order; group CN III, IV, VI together (all control eye movements).

CN I - Olfactory

  • Often omitted unless inferior frontal lobe disease (e.g., meningioma) suspected
  • Eyes closed - patient sniffs a mild odorant (toothpaste, coffee) and identifies it

CN II - Optic

  • Visual acuity: Snellen chart (with glasses/contacts)
  • Visual fields by confrontation:
    • Face patient at 0.6-1.0 m; hands at periphery of your own visual fields
    • Patient looks at center of your face; indicates when/where they see movement
    • Screen both eyes simultaneously; test each separately if abnormality found
  • Fundoscopy: Inspect optic disc, macula, vessels

CN III, IV, VI - Oculomotor, Trochlear, Abducens

  • Pupillary light reflex (CN II afferent / CN III efferent): direct & consensual
  • Extraocular movements: Ask patient to follow finger in an "H" pattern
    • CN III: up, down, medial gaze; elevates lid
    • CN IV: depression when eye adducted (reading)
    • CN VI: lateral gaze
  • Check for nystagmus and diplopia in eccentric gaze

CN V - Trigeminal

  • Sensation: Light touch in V1 (forehead), V2 (cheek), V3 (jaw) - both sides
  • Corneal reflex: Light cotton wisp to cornea (V1 afferent / CN VII efferent)
  • Motor: Clench jaw - palpate masseter; open jaw against resistance (pterygoids)
  • Jaw deviates toward the weak side with unilateral lesion

CN VII - Facial

  • Upper face (forehead wrinkling, eye closure) - spared in UMN lesions (bilateral cortical innervation)
  • Lower face (show teeth, puff cheeks, smile) - affected in both UMN and LMN lesions
  • Asymmetry is the key finding

CN VIII - Vestibulocochlear

  • Hearing: Whispered voice test; finger rub
  • Weber test: Tuning fork on vertex - lateralizes to affected ear (conductive loss) or good ear (sensorineural loss)
  • Rinne test: AC > BC (normal); BC > AC in conductive hearing loss

CN IX, X - Glossopharyngeal & Vagus

  • Observe palate elevation with "Aah" - uvula deviates away from the lesion
  • Gag reflex: Touched posterior pharynx (IX afferent / X efferent)
  • Assess voice quality (hoarseness = vagal lesion)
  • Swallowing evaluation

CN XI - Spinal Accessory

  • Shoulder shrug against resistance (trapezius - C3/C4 + CN XI)
  • Head rotation against resistance to each side (sternocleidomastoid)

CN XII - Hypoglossal

  • Inspect tongue for atrophy and fasciculations at rest
  • Protrusion: Tongue deviates toward the weak (LMN lesion) side
  • Strength: push tongue against inner cheek on each side

PART 3: MOTOR EXAMINATION

Bare minimum: Look for muscle atrophy + check tone. Assess upper limb: pronator drift + wrist/finger extensors. Lower limb: toe extensors.

A. Appearance

  • Inspect muscle groups under good lighting
  • Look for:
    • Fasciculations (LMN/anterior horn cell disease)
    • Atrophy or hypertrophy
    • Tenderness
  • Involuntary movements:
MovementWhen SeenAssociation
Tics, myoclonus, choreoathetosisAt restBasal ganglia / various
Pill-rolling tremorAt restParkinson's disease
Essential tremorMaintained postureFamilial/essential
Intention tremorDuring voluntary movementCerebellar disease

B. Tone

Test by passive movement of a relaxed limb (distract the patient to minimize active movement):
  • Upper limb: Rapid pronation-supination + flexion-extension at wrist
  • Lower limb (supine): Place hands behind knees, rapidly raise them - normal tone = heel drags before lifting; increased tone = heel lifts immediately
TypeCharacterLesion
SpasticityVelocity-dependent resistance ("clasp-knife")Corticospinal tract (UMN)
RigidityEqual resistance at all angles, all velocitiesExtrapyramidal (basal ganglia)
Cogwheel rigidityJerky interruptions in passive motionParkinsonism
Paratonia (Gegenhalten)Fluctuating resistanceFrontal lobe disease
Hypotonia/FlaccidityReduced resistanceLMN / peripheral nerve / cerebellar

C. Muscle Strength (MRC Scale)

GradeDescription
0No movement
1Flicker/trace contraction, no joint movement
2Movement with gravity eliminated
3Movement against gravity, not against resistance
4-Movement against mild resistance
4Movement against moderate resistance
4+Movement against strong resistance
5Full power
Key strength tests:
  • Pronator drift (very sensitive screen): Arms extended, parallel, eyes closed for 10 sec - pronation/flexion or asymmetry = weakness
  • Test major muscle groups in proximal → distal order

D. Reflexes

Deep Tendon Reflexes (DTRs):
ReflexLevel
BicepsC5, C6
BrachioradialisC5, C6
TricepsC7
Knee (patellar)L3, L4
Ankle (Achilles)S1
Grading:
GradeMeaning
0Absent
1Present but diminished
2Normoactive
3Increased
4Clonus
  • Reinforcement: Jendrassik maneuver (hook fingers and pull) for ankle reflex; teeth-clenching for upper limb
  • Test both sides sequentially; record minimum stimulus needed
Cutaneous (Superficial) Reflexes:
ReflexNormal ResponsePathwaySignificance if Absent
Plantar (Babinski)Plantar flexion of toesS1Extension = UMN lesion above S1
AbdominalUmbilicus moves toward stimulusT9-T12Absent with UMN lesions
CremastericIpsilateral testicular elevationL1, L2Absent with spinal cord/root lesion
Anal winkAnal sphincter contractionS2, S3, S4Important in cord/cauda equina injury
Primitive Reflexes (indicate frontal lobe disinhibition):
ReflexHow to ElicitResponse
Suck reflexTouch center of lips with tongue bladeSucking movement
Root reflexTouch corner of lipsLips move toward stimulus
Grasp reflexTouch palm between thumb and index fingerForced hand grasp
PalmomentalScratch palm diagonallyIpsilateral mentalis muscle contraction

PART 4: SENSORY EXAMINATION

Bare minimum: Light touch + temperature in each distal extremity. Double simultaneous stimulation. Romberg test.
Sensation is the most subjective part of the examination - requires a cooperative patient.

Primary Sensory Modalities (test all in each limb)

ModalityPathwayHow to Test
Light touchDorsal columns + spinothalamicWisp of cotton to skin
PainSpinothalamic (lateral)Broken wooden stick/safety pin; compare sharp vs. dull
TemperatureSpinothalamic (lateral)Warm vs. cool tubing/metal
VibrationDorsal columns128 Hz tuning fork on bony prominences (finger, toe, malleolus)
Joint position sense (proprioception)Dorsal columnsMove distal phalanx up or down; patient reports direction (eyes closed)
  • Test distal to proximal (abnormal findings guide how far to proceed)
  • Compare right vs. left, proximal vs. distal, upper vs. lower limbs

Cortical Sensory Modalities (require intact primary sensation + parietal lobe processing)

TestMethodWhat It Detects
GraphesthesiaWrite number/letter in palm; patient identifies itParietal lobe function
StereognosisPlace familiar object in hand (key, coin) - identify without lookingParietal lobe function
Two-point discriminationCalipers on fingertip - minimum distance perceived as two separate points (normal: 2-3 mm at fingertip)Discriminative touch
Double simultaneous stimulationTouch both hands simultaneously - patient reports bothExtinction = contralateral parietal lesion

Romberg Test (proprioception/dorsal column)

  • Patient stands with feet together, arms at sides
  • Eyes open first (balance maintained)
  • Then eyes closed: swaying/falling = positive Romberg (dorsal column or vestibular disorder)
  • A positive Romberg is not a cerebellar sign (cerebellar ataxia is present even with eyes open)

PART 5: GAIT & COORDINATION (CEREBELLAR)

Gait Observation

  • Ask patient to walk normally, then turn, then tandem walk (heel-to-toe)
Gait PatternDescriptionLocalization
Spastic (hemiplegic)Circumduction of the leg; arm flexedUMN/corticospinal
ParkinsonianShuffling, small steps, reduced arm swing, stoopedBasal ganglia
Ataxic (cerebellar)Wide-based, lurching, cannot tandem walkCerebellum
Sensory ataxicWide-based, worse with eyes closedDorsal columns
Steppage (foot drop)High-stepping to clear dropped footPeripheral nerve/LMN
WaddlingSide-to-side swayProximal myopathy

Cerebellar Tests

TestAbnormal FindingTerm
Finger-nose-fingerPast-pointing, tremor worsens near targetDysmetria, intention tremor
Heel-shin testIrregular, wavering movementDysmetria
Rapid alternating movements (pronation-supination)Irregular rhythm and amplitudeDysdiadochokinesia
Rebound testArm overshoots when suddenly releasedLoss of check

UMN vs. LMN - Key Distinguishing Features

FeatureUMN LesionLMN Lesion
ToneIncreased (spastic)Decreased (flaccid)
WeaknessPyramidal distributionFocal/segmental
Reflexes (DTRs)Increased (hyperreflexia)Decreased/absent
PlantarExtensor (Babinski +)Flexor (normal)
FasciculationsAbsentPresent
AtrophyMild (disuse)Prominent (neurogenic)
ClonusMay be presentAbsent

Quick Reference: Pupillary Findings in Coma

FindingLocalization
Reactive, symmetricalToxic-metabolic cause
Fixed, dilated unilaterallyCN III compression (herniation)
Pinpoint, reactive (with magnification)Pontine lesion
Midposition, fixedMidbrain lesion
Horner's syndrome (miosis, ptosis, anhidrosis)Sympathetic pathway disruption

Sources: Harrison's Principles of Internal Medicine 22nd Ed. (McGraw Hill, 2025), pp. 3423-3425; Goldman-Cecil Medicine International EditionThat covers the full systematic CNS examination. Here's a quick summary of what's included above:
5 major components covered:
  1. Higher Mental Functions - consciousness/GCS, orientation (person/place/time), speech vs. language, memory (immediate/short-term/long-term), insight, abstract thought, calculation, cognitive domain localization
  2. Cranial Nerves (CN I-XII) - step-by-step testing method, what each reflex tests, key abnormal findings (e.g., uvula deviation, tongue deviation direction, facial nerve UMN vs. LMN distinction)
  3. Motor System - appearance/fasciculations, tone types (spasticity vs. rigidity vs. cogwheel vs. paratonia), MRC 0-5 power grading, deep tendon reflexes with levels, cutaneous reflexes (Babinski, abdominal, cremasteric, anal), primitive reflexes (grasp, suck, palmomental)
  4. Sensory System - all 5 primary modalities with their pathways, cortical sensation (stereognosis, graphesthesia, two-point discrimination, double simultaneous stimulation), Romberg test
  5. Gait & Cerebellar - gait patterns with localization, finger-nose, heel-shin, dysdiadochokinesia, rebound
The UMN vs. LMN table and pupillary findings in coma are included as high-yield clinical summaries. Let me know if you want any section expanded further or a specific clinical scenario worked through.
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