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Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports

Journal of medical case reports, 2023-06, Vol.17 (1), p.244-244, Article 244

2023

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Clinical profile and aetiologies of delayed puberty: a 15 years’ experience from a tertiary centre in Sudan

Journal of Pediatric Endocrinology and Metabolism, 2022-07, Vol.35 (7), p.938-945

2022

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Clinical profile, etiology, and diagnostic challenges of primary adrenal insufficiency in Sudanese children: 14-years' experience from a resource limited setting

Journal of Pediatric Endocrinology and Metabolism, 2022-02, Vol.35 (2), p.231-237

2022

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47 A challenging case of refeeding-induced hyperglycemia

BMJ paediatrics open, 2024-05, Vol.8 (Suppl 4), p.A17-A18

2024

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Nutritional Challenges among African Refugee and Internally Displaced Children: A Comprehensive Scoping Review

Children (Basel), 2024-03, Vol.11 (3), p.318

2024

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Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children

International journal of pediatric endocrinology, 2020-11, Vol.2020 (1), p.1-21, Article 21

2020

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16 Monogenic diabetes; an experience from Sudan

BMJ paediatrics open, 2024-05, Vol.8 (Suppl 4), p.A5-A6

2024

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Improving COVID-19 Vaccine Uptake among Black Populations: A Systematic Review of Strategies

International journal of environmental research and public health, 2022-09, Vol.19 (19), p.11971

2022

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Central precocious puberty in Sudan: 10 years' experience of paediatric endocrinology centres

Sudanese journal of paediatrics, 2023, Vol.23 (2), p.145-152

2023

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Characterization of Hashimoto’s thyroiditis in Sudanese children: a cross-sectional study at Gaafar Ibn Auf Hospital, Khartoum

The Pan African medical journal, 2023, Vol.44

2023

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Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan

Pediatric diabetes, 2024-02, Vol.2024, p.1-10

2024

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Characterization of Hashimoto´s thyroiditis in Sudanese children: a cross-sectional study at Gaafar Ibnauf Hospital, Khartoum

The Pan African medical journal, 2023, Vol.44, p.86-86

2023

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THU232 Genetic Study In A Series Of 29 Triple A Syndrome Patients From 19 Sudanese Families - Identification Of Two Novel AAAS Mutations

Journal of the Endocrine Society, 2023-10, Vol.7 (Supplement_1)

2023

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Challenges in diagnosis and management of neonatal hyperparathyroidism in a resource-limited country: a case series from a Sudanese family

The Pan African medical journal, 2021-10, Vol.40

2021

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RF33 | PSAT69 A Combined Candidate Gene/Whole Exome Sequencing Approach Permits a Rapid Genetic Diagnosis for >81% Individuals with Primary Adrenal Insufficiency

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A140-A141

2022

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A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees

Genes, 2022-04, Vol.13 (4), p.657

2022

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Salivary CXCL13 in relation to scintigraphy in early detection of secondary Sjogren’s syndrome

Egyptian Rheumatology and Rehabilitation, 2018-10, Vol.45 (4), p.153-158

2018

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Central precocious puberty in Sudan: ten years' experience of pediatric endocrinology centers

Sudanese journal of paediatrics, 2023, p.145-152

2023

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WES as a tool for differential diagnosis of adrenal insufficiency in sudanese children

Endocrine Abstracts, 2024-09

2024

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Genetic aetiology of primary adrenal insufficiency in Sudan

Endocrine Abstracts, 2023-10

2023

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Genetic Aetiology of Primary Adrenal Insufficiency in Sudan

Endocrine Abstracts, 2023-05

2023

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A rapid genetic diagnosis for >80% individuals with non-CAH Primary Adrenal Insufficiency is achievable by candidate gene sequencing combined with WES

Endocrine Abstracts, 2022-05

2022

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Aetiologies and clinical patterns of hypopituitarism in Sudanese children

Sudanese journal of paediatrics, 2021, Vol.21 (1), p.53-60

2021

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Endocardiomiofibrose idiopática complicada com a realização de procedimento invasivo: relato de caso

Revista Eletrônica Acervo Científico, 2020-03, Vol.9, p.e3286

2020

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Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports

Clinical profile and aetiologies of delayed puberty: a 15 years’ experience from a tertiary centre in Sudan

Clinical profile, etiology, and diagnostic challenges of primary adrenal insufficiency in Sudanese children: 14-years' experience from a resource limited setting

47 A challenging case of refeeding-induced hyperglycemia

Nutritional Challenges among African Refugee and Internally Displaced Children: A Comprehensive Scoping Review

Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village

Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children

16 Monogenic diabetes; an experience from Sudan

Improving COVID-19 Vaccine Uptake among Black Populations: A Systematic Review of Strategies

Central precocious puberty in Sudan: 10 years' experience of paediatric endocrinology centres

Characterization of Hashimoto’s thyroiditis in Sudanese children: a cross-sectional study at Gaafar Ibn Auf Hospital, Khartoum

Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan

Characterization of Hashimoto´s thyroiditis in Sudanese children: a cross-sectional study at Gaafar Ibnauf Hospital, Khartoum

THU232 Genetic Study In A Series Of 29 Triple A Syndrome Patients From 19 Sudanese Families - Identification Of Two Novel AAAS Mutations

Challenges in diagnosis and management of neonatal hyperparathyroidism in a resource-limited country: a case series from a Sudanese family

RF33 | PSAT69 A Combined Candidate Gene/Whole Exome Sequencing Approach Permits a Rapid Genetic Diagnosis for >81% Individuals with Primary Adrenal Insufficiency

A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees

Salivary CXCL13 in relation to scintigraphy in early detection of secondary Sjogren’s syndrome

Central precocious puberty in Sudan: ten years' experience of pediatric endocrinology centers

WES as a tool for differential diagnosis of adrenal insufficiency in sudanese children

Genetic aetiology of primary adrenal insufficiency in Sudan

Genetic Aetiology of Primary Adrenal Insufficiency in Sudan

A rapid genetic diagnosis for >80% individuals with non-CAH Primary Adrenal Insufficiency is achievable by candidate gene sequencing combined with WES

Aetiologies and clinical patterns of hypopituitarism in Sudanese children

Endocardiomiofibrose idiopática complicada com a realização de procedimento invasivo: relato de caso

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