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	35,876	1,178	37,054
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	30,718	1,254	31,972
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	29,644	829	30,473
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	28,694	853	29,547
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	22,268	801	23,069
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	21,719	837	22,556
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	20,988	637	21,625
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	20,431	914	21,345
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	18,193	1,380	19,573
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	17,981	1,217	19,198
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	18,310	755	19,065
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	17,716	1,184	18,900
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	15,821	2,853	18,674
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	17,720	875	18,595
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	17,268	1,001	18,269
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	16,973	566	17,539
Case Report Hypopituitarism secondary to pediatric traumatic brain injury – A need for active vigilance Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_39_2024	15,336	820	16,156
Original Article Depression and anxiety screening for adolescents with type 1 diabetes: A quality improvement project Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_18_2024	15,238	723	15,961
Editorial Editor’s page Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_31_2024	15,353	599	15,952
Ped Endo Journal Scan Ped Endo Journal Scan Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_51_2024	15,124	671	15,795
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	13,874	1,382	15,256
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	13,296	1,123	14,419
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	12,817	1,105	13,922
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	12,338	822	13,160
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	11,998	917	12,915
Editorial Editor’s Page Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_53_2024	12,345	325	12,670
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	11,779	829	12,608
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	10,319	703	11,022
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	9,809	1,178	10,987
Guest Editorial COVID-19 pandemic and new-onset diabetes mellitus – The evidence for a causal relationship Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_49_2024	10,609	300	10,909
Editorial Commentary COVID-19 and the surge in youth diabetes: Fleeting effect or lasting consequence? Full text \| PDF Year: 2024, Volume: 4, Issue: 2, May-August DOI: 10.25259/JPED_52_2024	10,473	308	10,781
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	5,969	2,694	8,663
Case Series 17Beta-hydroxysteroid dehydrogenase type 3 deficiency: A single-center case series experience Full text \| PDF Year: 2024, Volume: 4, Issue: 3, September-December DOI: 10.25259/JPED_29_2024	8,082	179	8,261
President’s Page President’s page Full text \| PDF Year: 2024, Volume: 4, Issue: 1, January-April DOI: 10.25259/JPED_4_1_1	7,643	432	8,075
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	6,847	640	7,487
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	4,757	2,543	7,300
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	5,025	2,101	7,126
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	4,492	2,515	7,007
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	4,207	2,796	7,003
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	4,333	2,631	6,964
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	4,374	2,264	6,638
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	3,895	2,719	6,614
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	4,065	2,444	6,509
Original Article Psychological effects of precocious puberty on young girls and their mothers Full text \| PDF Year: 2024, Volume: 4, Issue: 3, September-December DOI: 10.25259/JPED_16_2024	6,252	194	6,446
News ISPAE elections ISPAE Office bearers 2023-24 Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August	4,006	2,432	6,438
Editorial Editor’s page Full text \| PDF Year: 2022, Volume: 2, Issue: 2, May-August DOI: 10.25259/JPED_40_2022	3,936	2,490	6,426
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	4,103	2,258	6,361
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	3,803	2,543	6,346
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	4,371	1,923	6,294
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	3,950	2,173	6,123

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

Unusual clustering of comorbidities in a child with Down syndrome

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

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

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

Ped Endo Journal Scan

Neurodevelopmental delay as the initial presentation of thyroid hormone resistance syndrome

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

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

Late bloomer: Delayed diagnosis of Prader-Willi syndrome

Ped Endo Journal Scan

Pediatric endocrinology training in India

Early neurological association in a young child with Wolfram syndrome

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

Aromatase inhibitors for idiopathic short stature: A Commentary

Hypopituitarism secondary to pediatric traumatic brain injury – A need for active vigilance

Depression and anxiety screening for adolescents with type 1 diabetes: A quality improvement project

Editor’s page

Ped Endo Journal Scan

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

Editor’s Page

Late presentation of lipoid congenital adrenal hyperplasia in a phenotypic male

Delaying the growth plate closure to augment height

Etiology and outcome of hypoglycemia in young children: Indian perspective

COVID-19 pandemic and new-onset diabetes mellitus – The evidence for a causal relationship

COVID-19 and the surge in youth diabetes: Fleeting effect or lasting consequence?

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

17Beta-hydroxysteroid dehydrogenase type 3 deficiency: A single-center case series experience

President’s page

Genetic diagnosis in XY disorders of sex development

A case of McCune–Albright syndrome hiding in the bones

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

Genetics for the pediatric endocrinologists – 1

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

Ped endo journal scan

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

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

Psychological effects of precocious puberty on young girls and their mothers

ISPAE Office bearers 2023-24

Editor’s page

Laron syndrome in South Indian children – A descriptive study

Congenital aromatase deficiency – A virilizing masquerade!

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

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

**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**