Verma P - Search Results

1

Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation.

Kantaputra PN, Kapoor S, Verma P, Kaewgahya M, Kawasaki K, Ohazama A, Ketudat Cairns JR. Kantaputra PN, et al. Among authors: verma p. Eur J Med Genet. 2017 Dec;60(12):695-700. doi: 10.1016/j.ejmg.2017.09.005. Epub 2017 Sep 14. Eur J Med Genet. 2017. PMID: 28917830

2

Frontotemporal Atrophy: Presenting Sign in Infantile Cobalamin Deficiency.

Vats P, Verma P, Varughese B, Kumar S, Kapoor S. Vats P, et al. Among authors: verma p. Indian J Pediatr. 2018 Jul;85(7):565-566. doi: 10.1007/s12098-017-2542-7. Epub 2017 Nov 23. Indian J Pediatr. 2018. PMID: 29170924 No abstract available.

3

Split hand-foot malformation and a novel WNT10B mutation.

Kantaputra PN, Kapoor S, Verma P, Intachai W, Ketudat Cairns JR. Kantaputra PN, et al. Among authors: verma p. Eur J Med Genet. 2018 Jul;61(7):372-375. doi: 10.1016/j.ejmg.2018.02.001. Epub 2018 Feb 7. Eur J Med Genet. 2018. PMID: 29427788

4

An Optimal Capillary Screen Cut-off of Thyroid Stimulating Hormone for Diagnosing Congenital Hypothyroidism: Data from a Pilot Newborn Screening Program in Delhi.

Verma P, Kapoor S, Kalaivani M, Vats P, Yadav S, Jain V, Thelma BK; Science and Engineering Research Board – Newborn Screening Initiative Group (SERB-NBS) members. Verma P, et al. Indian Pediatr. 2019 Apr 15;56(4):281-286. Indian Pediatr. 2019. PMID: 31064895 Free article.

5

Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies in a Young Infant: First Case Entity of Casamassima-Morton-Nance Syndrome from Asia.

Lourembam R, Gupta MK, Sherwani P, Verma PK. Lourembam R, et al. Among authors: verma pk. J Pediatr Genet. 2022 Jul 11;13(3):227-231. doi: 10.1055/s-0042-1749367. eCollection 2024 Sep. J Pediatr Genet. 2022. PMID: 39086454 Free PMC article.

6

Systemic Pseudohypoaldosteronism Type 1 Due to a Novel Mutation in SCNN1B Gene: A Case Report.

Joshi K, Verma PK, Barman M. Joshi K, et al. EJIFCC. 2022 Oct 28;33(3):268-273. eCollection 2022 Oct. EJIFCC. 2022. PMID: 36447799 Free PMC article.

7

Utility of MLPA in mutation analysis and carrier detection for Duchenne muscular dystrophy.

Verma PK, Dalal A, Mittal B, Phadke SR. Verma PK, et al. Indian J Hum Genet. 2012 Jan;18(1):91-4. doi: 10.4103/0971-6866.96667. Indian J Hum Genet. 2012. PMID: 22754229 Free PMC article.

8

Association of serum zinc levels and symptom control of asthma in children and adolescents- a prospective observational study.

Rajkumar S, Bhat NK, Kumar V, Bolia R, Verma PK, Kumar M, Chacham S, Mirza AA. Rajkumar S, et al. Eur J Pediatr. 2023 Jan;182(1):141-147. doi: 10.1007/s00431-022-04656-9. Epub 2022 Oct 14. Eur J Pediatr. 2023. PMID: 36229694 Free PMC article.

9

Thurston syndrome with thalassaemia: a rare case devising a novel molecular and phenotypic variation.

Ks A, Bansal A, Verma PK, Bhat NK. Ks A, et al. BMJ Case Rep. 2023 Dec 30;16(12):e253086. doi: 10.1136/bcr-2022-253086. BMJ Case Rep. 2023. PMID: 38160027

10

What is your diagnosis?

Chawla L, Jindal A, Verma PK, Bahadur A, Prateek S. Chawla L, et al. J Turk Ger Gynecol Assoc. 2020 Sep 3;21(3):213-215. doi: 10.4274/jtgga.galenos.2020.2019.0184. Epub 2020 Jun 10. J Turk Ger Gynecol Assoc. 2020. PMID: 32517430 Free PMC article. No abstract available.

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