Overview
Kausik Mandal practices in Lucknow, India. Mandal is rated as an Experienced expert by MediFind in the treatment of CHST3-Related Skeletal Dysplasia. Their top areas of expertise are Pycnodysostosis, Bidirectional Tachycardia, Nephrocalcinosis, and X-Linked Cardiac Valvular Dysplasia.
Their clinical research consists of co-authoring 88 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 1 article in the study of CHST3-Related Skeletal Dysplasia.
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Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Bidirectional TachycardiaMandal isDistinguished. Learn about Bidirectional Tachycardia.
- PycnodysostosisMandal isDistinguished. Learn about Pycnodysostosis.
- Advanced
- Bartter SyndromeMandal isAdvanced. Learn about Bartter Syndrome.
- Brachydactyly Mononen Type
- ChondrodystrophyMandal isAdvanced. Learn about Chondrodystrophy.
- Cockayne Syndrome Type 1Mandal isAdvanced. Learn about Cockayne Syndrome Type 1.
- Congenital Nephrotic Syndrome
- Distal Renal Tubular Acidosis
- Experienced
- Absence SeizureMandal isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeMandal isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acid Sphingomyelinase Deficiency (ASMD)
- Acromesomelic DysplasiaMandal isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type