Journal of Pediatric Endocrinology and Diabetes

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Case Report *Refractory rickets: A case of X-linked hypophosphatemic rickets (PHEX* gene variation)** Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_43_2023	35,448	512	35,960
Systematic Review Efficacy and safety of aromatase inhibitors in the management of idiopathic short stature: A meta-analysis Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_42_2023	30,063	587	30,650
Invited Review Molecular mechanisms underlying congenital hyperinsulinemia of infancy and its relevance to management – A review Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_25_2024	21,132	244	21,376
Ped Endo Journal Scan Ped Endo Journal Scan Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_33_2024	20,809	224	21,033
Clinical Images/Spotters Unusual clustering of comorbidities in a child with Down syndrome Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_11_2024	18,342	278	18,620
Clinical Images/Spotters A boy with type 1 diabetes who could not do ‘Namaste’! Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_2_2024	17,679	724	18,403
Case Report Pseudohypoparathyroidism type 1A and Albright hereditary osteodystrophy: A genetic conundrum of multiple hormonal resistances in a family Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_19_2023	17,706	660	18,366
Clinical Images/Spotters Late bloomer: Delayed diagnosis of Prader-Willi syndrome Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_19_2024	18,017	240	18,257
Ped Endo Journal Scan Ped Endo Journal Scan Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_4_2024	17,467	756	18,223
Letter to Editor Early neurological association in a young child with Wolfram syndrome Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_20_2023	17,455	643	18,098
Original Article Patterns of incidence and characteristics of youth with new-onset diabetes mellitus during the COVID era Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_5_2024	17,454	277	17,731
Case Report Diabetic striatopathy – A rare manifestation of type 1 diabetes in children – A case report Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_10_2024	16,952	316	17,268
Pediatric Endocrine Trainees Section (Open-Forum) Pediatric endocrinology training in India Full text \| PDF Year: 2021, Volume: 1, Issue: 1, September-December DOI: 10.25259/JPED_12_2021	14,115	2,098	16,213
Invited Editorial Commentary Aromatase inhibitors for idiopathic short stature: A Commentary Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_26_2024	16,049	159	16,208
Editorial Editor’s page Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_31_2024	15,157	152	15,309
Case Report Acute insulin-induced hypoglycemia in twin neonates Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_39_2023	13,454	700	14,154
Case Report Postprandial hypoinsulinemic hypoglycemia as a clue to hidden purging behavior in an adolescent boy with disordered eating Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_40_2023	12,999	616	13,615
Original Article Etiology and outcome of hypoglycemia in young children: A retrospective cohort study Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_29_2023	12,338	602	12,940
Editorial Commentary Evaluation of the etiology and outcome of hypoglycemia in young children – A challenging task Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_7_2024	12,126	616	12,742
Case Report Clinical characteristics and management of gonadotropin-independent precocious puberty in McCune–Albright syndrome in children – A case series from a tertiary care center, Sri Lanka Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_41_2023	11,755	306	12,061
Case Report Late presentation of lipoid congenital adrenal hyperplasia in a phenotypic male Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_15_2024	11,522	248	11,770
Case Series Neonatal hypoglycemia: A review with focus on practical challenges and recent updates on management Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_20_2024	11,469	207	11,676
Editorial Commentary Etiology and outcome of hypoglycemia in young children: Indian perspective Full text \| PDF Year: 2023, Volume: 3, Issue: 3, September-December DOI: 10.25259/JPED_8_2024	9,450	637	10,087
Case Report Neurodevelopmental delay as the initial presentation of thyroid hormone resistance syndrome Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_3_2024	8,977	91	9,068
President’s Page President’s page Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_4_1_1	7,451	115	7,566
Invited Review Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_38_2022	5,167	1,950	7,117
Invited Editorial Commentary Delaying the growth plate closure to augment height Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_22_2024	6,603	261	6,864
Ped Endo Journal Scan Ped endo journal scan Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_28_2022	4,124	2,202	6,326
Invited Review – Genetics for the Pediatric Endocrinologists – 7 Genetic diagnosis in XY disorders of sex development Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_42_2024	6,149	141	6,290
Original Article Treatment of diabetic ketoacidosis with subcutaneous regular insulin in a non-ICU setting is effective and economical: A single-center experience Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_19_2022	4,585	1,651	6,236
Editorial Type 1 diabetes in limited resource settings: Where are we and where do we need to go? Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_39_2022	3,854	2,140	5,994
Case Report A case of McCune–Albright syndrome hiding in the bones Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_22_2022	4,330	1,656	5,986
News ISPAE elections ISPAE Office bearers 2023-24 Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August	3,787	2,143	5,930
Invited Review Genetics for the pediatric endocrinologists – 1 Full text \| PDF Year: 2022, Volume: 2, Issue: 1, January-April DOI: 10.25259/JPED_6_2022	3,863	1,993	5,856
Original Article A study on normalization of hypothyroxinemia in neonates below 34 weeks of gestation Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_4_2022	3,806	2,038	5,844
Case Report *Allan-Herndon-Dudley syndrome: Report of a novel pathogenic variant in MCT8* gene** Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_5_2022	4,016	1,524	5,540
Original Article Turkish children with new-onset type 1 diabetes mellitus had more severe clinical presentation during COVID-19 pandemic Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_20_2022	3,734	1,802	5,536
Editorial Editor’s page Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_40_2022	3,646	1,879	5,525
Invited Review – Genetics for the Pediatric Endocrinologist 3 Comprehensive Overview of Congenital Adrenal Hyperplasia and its Genetic Diagnosis Among Children and Adolescents Full text \| PDF Year: 2022, Volume: 2, Issue: 3, September-December DOI: 10.25259/JPED_4_2023	3,950	1,557	5,507
Case Report *Neonatal diabetes mellitus with congenital hypothyroidism (NDH) syndrome caused by GLIS3* mutation: A case report and review of literature** Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_24_2022	3,514	1,856	5,370
Editorial Bone health in children with type 1 diabetes mellitus Full text \| PDF Year: 2022, Volume: 2, Issue: 1, January-April DOI: 10.25259/JPED_11_2022	3,179	2,136	5,315
Clinical Images Short child with hypermobility of shoulder joint: A rare case of skeletal dysplasia Full text \| PDF Year: 2022, Volume: 2, Issue: 1, January-April DOI: 10.25259/JPED_22_2021	3,415	1,891	5,306
Case Report Congenital aromatase deficiency – A virilizing masquerade! Full text \| PDF Year: 2022, Volume: 2, Issue: 1, January-April DOI: 10.25259/JPED_26_2021	3,414	1,863	5,277
Pediatric Endocrine Trainees Section (Open-Forum) Endocrine services for children disrupted by COVID-19 – A fellow’s perspective Full text \| PDF Year: 2022, Volume: 2, Issue: 1, January-April DOI: 10.25259/JPED_3_2022	3,105	1,985	5,090
Book Review Advanced Pediatric Endocrinology Full text \| PDF Year: 2021, Volume: 1, Issue: 1, September-December	2,920	2,123	5,043
Case Report *Pseudohypoparathyroidism-Ib due to novel heterozygous stop gain mutation in exon 8 of STX16* gene: A case report** Full text \| PDF Year: 2021, Volume: 1, Issue: 1, September-December DOI: 10.25259/JPED_3_2021	3,012	2,025	5,037
Original Article Laron syndrome in South Indian children – A descriptive study Full text \| PDF Year: 2022, Volume: 2, Issue: 3, September-December DOI: 10.25259/JPED_17_2022	3,414	1,595	5,009
Original Article Type 1 diabetes self-care in urban schools in India Full text \| PDF Year: 2021, Volume: 1, Issue: 1, September-December DOI: 10.25259/JPED_6_2021	3,239	1,742	4,981
Ped Endo Journal Scan Ped Endo Journal Scan Full text \| PDF Year: 2022, Volume: 2, Issue: 1, January-April DOI: 10.25259/JPED_9_2022	3,119	1,783	4,902
Book Review Pediatric Endocrinology – An examination-oriented simplified textbook Full text \| PDF Year: 2022, Volume: 2, Issue: 3, September-December DOI: 10.25259/JPED_8_2023	3,293	1,602	4,895

Most Viewed Articles

Refractory rickets: A case of X-linked hypophosphatemic rickets (PHEX gene variation)

Efficacy and safety of aromatase inhibitors in the management of idiopathic short stature: A meta-analysis

Molecular mechanisms underlying congenital hyperinsulinemia of infancy and its relevance to management – A review

Ped Endo Journal Scan

Unusual clustering of comorbidities in a child with Down syndrome

A boy with type 1 diabetes who could not do ‘Namaste’!

Pseudohypoparathyroidism type 1A and Albright hereditary osteodystrophy: A genetic conundrum of multiple hormonal resistances in a family

Late bloomer: Delayed diagnosis of Prader-Willi syndrome

Ped Endo Journal Scan

Early neurological association in a young child with Wolfram syndrome

Patterns of incidence and characteristics of youth with new-onset diabetes mellitus during the COVID era

Diabetic striatopathy – A rare manifestation of type 1 diabetes in children – A case report

Pediatric endocrinology training in India

Aromatase inhibitors for idiopathic short stature: A Commentary

Editor’s page

Acute insulin-induced hypoglycemia in twin neonates

Postprandial hypoinsulinemic hypoglycemia as a clue to hidden purging behavior in an adolescent boy with disordered eating

Etiology and outcome of hypoglycemia in young children: A retrospective cohort study

Evaluation of the etiology and outcome of hypoglycemia in young children – A challenging task

Clinical characteristics and management of gonadotropin-independent precocious puberty in McCune–Albright syndrome in children – A case series from a tertiary care center, Sri Lanka

Late presentation of lipoid congenital adrenal hyperplasia in a phenotypic male

Neonatal hypoglycemia: A review with focus on practical challenges and recent updates on management

Etiology and outcome of hypoglycemia in young children: Indian perspective

Neurodevelopmental delay as the initial presentation of thyroid hormone resistance syndrome

President’s page

Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents

Delaying the growth plate closure to augment height

Ped endo journal scan

Genetic diagnosis in XY disorders of sex development

Treatment of diabetic ketoacidosis with subcutaneous regular insulin in a non-ICU setting is effective and economical: A single-center experience

Type 1 diabetes in limited resource settings: Where are we and where do we need to go?

A case of McCune–Albright syndrome hiding in the bones

ISPAE Office bearers 2023-24

Genetics for the pediatric endocrinologists – 1

A study on normalization of hypothyroxinemia in neonates below 34 weeks of gestation

Allan-Herndon-Dudley syndrome: Report of a novel pathogenic variant in MCT8 gene

Turkish children with new-onset type 1 diabetes mellitus had more severe clinical presentation during COVID-19 pandemic

Editor’s page

Comprehensive Overview of Congenital Adrenal Hyperplasia and its Genetic Diagnosis Among Children and Adolescents

Neonatal diabetes mellitus with congenital hypothyroidism (NDH) syndrome caused by GLIS3 mutation: A case report and review of literature

Bone health in children with type 1 diabetes mellitus

Short child with hypermobility of shoulder joint: A rare case of skeletal dysplasia

Congenital aromatase deficiency – A virilizing masquerade!

Endocrine services for children disrupted by COVID-19 – A fellow’s perspective

Advanced Pediatric Endocrinology

Pseudohypoparathyroidism-Ib due to novel heterozygous stop gain mutation in exon 8 of STX16 gene: A case report

Laron syndrome in South Indian children – A descriptive study

Type 1 diabetes self-care in urban schools in India

Ped Endo Journal Scan

Pediatric Endocrinology – An examination-oriented simplified textbook

**Refractory rickets: A case of X-linked hypophosphatemic rickets (PHEX gene variation)**

**Allan-Herndon-Dudley syndrome: Report of a novel pathogenic variant in MCT8 gene**

**Neonatal diabetes mellitus with congenital hypothyroidism (NDH) syndrome caused by GLIS3 mutation: A case report and review of literature**

**Pseudohypoparathyroidism-Ib due to novel heterozygous stop gain mutation in exon 8 of STX16 gene: A case report**