Suchergebnisse - "Mandal, Kausik"

PubPharm (28)

1

Congenital nephrotic syndrome with diffuse mesangial sclerosis caused by compound heterozygous mutation in LAMA5 gene

enthalten in: Pediatric nephrology (Berlin, Germany) | 2024

von Deepthi, B. | Sivakumar, R. | Krishnasamy, S. | +3

2

Hydrometrocolpos : antenatal diagnosis and postnatal management

enthalten in: BMJ case reports | 2023

von Singh, A. | Mandelia, A. | Naranje, K. | +1

3

A Hypotonic Neonate

enthalten in: NeoReviews | 2022

von Roy, A. | Naranje, K. | Mandal, K. | +1

4

Rare case of dual diagnosis in consanguineous family : a case report

enthalten in: Clinical dysmorphology | 2021

von Agrawal, N. | Mandal, K.

5

A Rare Etiology of Hypocalcemic Seizures in Adulthood : Clues to Diagnosis from Facial Dysmorphism

enthalten in: Neurology India | 2021

von Batra, N. | Kant, R. | Mandal, K. | +1

6

Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia

enthalten in: Annals of hematology | 2020

von Tripathi, P. | Agarwal, S. | Gupta, A. | +1

7

Vici Syndrome with a Novel Mutation in EPG5

enthalten in: Indian pediatrics | 2019

von Moirangthem, A. | Mandal, K. | Ghosh, A. | +1

8

Unusual Cause of Bidirectional Ventricular Rhythm

enthalten in: JACC. Case reports | 2019

von Chakraborty, P. | Isser, H. | Arava, S. | +3

9

Expanding the phenotype in autosomal dominant mental retardation-24 : a novel variation in DEAF1 gene

enthalten in: Clinical dysmorphology | 2019

von Sharma, P. | Gambhir, P. | Phadke, S. | +1

10

Phenotypic characterization of derivative 22 syndrome : case series and review

enthalten in: Journal of genetics | 2018

von Saxena, D. | Srivastava, P. | Tuteja, M. | +2