Biochemistry by Dr Rajesh Jambhulkar

Sickle cell anemia ECE

Porphyria cutanea tarda ECE

Phenylketonuria ECE

Galactosemia ECE

Homocystinuria ECE

Maple syrup urine disease ECE

G6PD deficiency ECE

Alkaptonuria ECE

Primary hyperoxaluria ECE

Albinism ECE

Hereditary Fructose Intolerance ECE

beta thalassemia major ECE

Congenital erythropoietic porphyria ECE

Neonatal physiological jaundice ECE

Crigler najjar type 1 and 2, Gilbert syndrome

Dubin Johnson syndrome, Rotor syndrome

Parkinson's disease ECE

Carcinoid syndrome ECE

Hartnups disease ECE

Jamaican vomiting sickness ECE

Tangiers disease ECE

Type IIa Familial hypercholesterolemia ECE

Type I Familial hyperchylomicronemia ECE

Zellweger syndrome ECE

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Biochemistry rapid revision handwritten notes @Rs 596

Behind scene

Biochemistry Rapid Revision Handwritten Notes

Pellagra- Early clinical exposure

Digestion and absorption of Lipids

G6PD Deficiency- HMP Shunt- Clinical case

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LAQ- Regulation of Gene Expression in Eukaryotes

Quiz Result declaration LIVE

Tricolor Tests in Biochemistry- Orange, White and Green

[Fructose Metabolism in 3 Min ] Hereditary fructose intolerance- Clinical case discussion

Biochem notes-Premium version [Colored]- Rapid Revision

50 Important cases Rapid Revision- Key points

Pocket Biochemistry- MBBS Biochemistry App

Rothera's test live demo- for Ketone bodies

1 MCQ in 1 minute-Glucose transporters GLUTs

1 MCQ in 1 minute- Marker enzymes for cell organelles

Digestion and absorption of proteins and disorders

Homocystinuria- Inborn error of Methionine and cysteine metabolism

Best Luck for University Exams

NExT- PG Entrance Exam-Understanding the Draft NMC

Digestion of carbohydrates

Why GAGs are Slippery in Nature?

Important Topics Biochemistry MBBS First Year

How to Prepare for Biochemistry [Hindi]