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Rahul Mahajan

Showing results (171-180 of 210) with videos related to

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The Australasian Journal of Dermatology|April 22, 2024
A photo-distributed rash and eczematous eruptions in two siblings-A diagnostic conundrumKittu Malhi, Akash Mustari, Sukhdeep Singh, et al.
Indian Journal of Dermatology, Venereology and Leprology|August 17, 2024
Co-occurring livedoid vasculopathy and limited cutaneous systemic sclerosis associated gangrene successfully managed with alprostadil and aspirinNarayanan Baskaran, Akash Mustari, Kittu Malhi, et al.
Clinical and Experimental Dermatology|March 6, 2022
Atypical Wiskott-Aldrich syndrome without thrombocytopenia partially responding to omalizumab therapyPriyansh Gupta, Kirutika Subburaj, Ankur Jindal, et al.
Indian Journal of Dermatology|August 25, 2020
Dermoscopy of Follicular Dowling-Degos DiseaseGarima Dabas, Rahul Mahajan, T P Afra, et al.
Pediatric Dermatology|August 14, 2023
Expanding the clinical and immunological phenotype of prolidase deficiency: A case reportSuprit Basu, Prabal Barman, Jhumki Das, et al.
Clinical and Experimental Dermatology|September 11, 2025
Clinico-demographic characteristics of pemphigus foliaceus: Retrospective analysis of clinic-based data of 103 patients in a non-endemic locationDipankar De, Apoorva Sharma, Vinod Hanumanthu, et al.
International Review of Neurobiology|October 2, 2015
Unifying Mechanism of Controlling Kir3 Channel Activity by G Proteins and PhosphoinositidesDiomedes E Logothetis, Rahul Mahajan, Scott K Adney, et al.
American Journal of Medical Genetics. Part A|October 28, 2020
Clericuzio-type poikiloderma with neutropenia in a patient from IndiaAnuradha Bishnoi, Manu Jamwal, Reena Das, et al.
Scientific Reports|August 20, 2021
The severity of malnutrition in children with epidermolysis bullosa correlates with disease severitySeema Manjunath, Rahul Mahajan, Dipankar De, et al.
Archives of Dermatological Research|October 3, 2022
A cross-sectional study to find association of VDR gene polymorphism with non-syndromic congenital ichthyosis and with vitamin D deficiencyHitaishi Kaushik, Rahul Mahajan, Garima Dabas, et al.
Pageof 21

Showing results (171-180 of 210) with videos related to

Sort By:
Pageof 21
The Australasian Journal of Dermatology|April 22, 2024
A photo-distributed rash and eczematous eruptions in two siblings-A diagnostic conundrumKittu Malhi, Akash Mustari, Sukhdeep Singh, et al.
Indian Journal of Dermatology, Venereology and Leprology|August 17, 2024
Co-occurring livedoid vasculopathy and limited cutaneous systemic sclerosis associated gangrene successfully managed with alprostadil and aspirinNarayanan Baskaran, Akash Mustari, Kittu Malhi, et al.
Clinical and Experimental Dermatology|March 6, 2022
Atypical Wiskott-Aldrich syndrome without thrombocytopenia partially responding to omalizumab therapyPriyansh Gupta, Kirutika Subburaj, Ankur Jindal, et al.
Indian Journal of Dermatology|August 25, 2020
Dermoscopy of Follicular Dowling-Degos DiseaseGarima Dabas, Rahul Mahajan, T P Afra, et al.
Pediatric Dermatology|August 14, 2023
Expanding the clinical and immunological phenotype of prolidase deficiency: A case reportSuprit Basu, Prabal Barman, Jhumki Das, et al.
Clinical and Experimental Dermatology|September 11, 2025
Clinico-demographic characteristics of pemphigus foliaceus: Retrospective analysis of clinic-based data of 103 patients in a non-endemic locationDipankar De, Apoorva Sharma, Vinod Hanumanthu, et al.
International Review of Neurobiology|October 2, 2015
Unifying Mechanism of Controlling Kir3 Channel Activity by G Proteins and PhosphoinositidesDiomedes E Logothetis, Rahul Mahajan, Scott K Adney, et al.
American Journal of Medical Genetics. Part A|October 28, 2020
Clericuzio-type poikiloderma with neutropenia in a patient from IndiaAnuradha Bishnoi, Manu Jamwal, Reena Das, et al.
Scientific Reports|August 20, 2021
The severity of malnutrition in children with epidermolysis bullosa correlates with disease severitySeema Manjunath, Rahul Mahajan, Dipankar De, et al.
Archives of Dermatological Research|October 3, 2022
A cross-sectional study to find association of VDR gene polymorphism with non-syndromic congenital ichthyosis and with vitamin D deficiencyHitaishi Kaushik, Rahul Mahajan, Garima Dabas, et al.
Pageof 21