H. Al-Hindi

发表

Curcumin inhibits the Sonic Hedgehog signaling pathway and triggers apoptosis in medulloblastoma cells

A. Aboussekhra, Y. Khafaga, M. Elamin, 2009, Molecular carcinogenesis.

HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern Population.

A. Alzahrani, H. Al-Hindi, Ebtesam Qasem, 2016, Thyroid : official journal of the American Thyroid Association.

Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia

B. Meyer, D. Monies, H. Al-Hindi, 2022, Frontiers in Neuroscience.

LGMD 1 D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB 6 mutation

B. Meyer, S. Bohlega, D. Monies, 2019 .

LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

B. Meyer, S. Bohlega, D. Monies, 2018, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

A. Bawazir, H. Al-Hindi, I. Althubaiti, 2020 .

Uncommon TERT Promoter Mutations in Pediatric Thyroid Cancer.

M. Xing, A. Alzahrani, H. Al-Hindi, 2016, Thyroid : official journal of the American Thyroid Association.

Comparison of differentiated thyroid cancer in children and adolescents (≤20 years) with young adults

A. Alzahrani, H. Al-Hindi, B. B. Sadiq, 2016, Clinical endocrinology.

Papillary Thyroid Cancer and a TERT Promotor Mutation-positive Paraganglioma in a Patient With a Germline SDHB Mutation

A. Alzahrani, H. Al-Hindi, Meshael M. Alswailem, 2022, Journal of the Endocrine Society.

Genetic Alterations in Pediatric Thyroid Cancer Using a Comprehensive Childhood Cancer Gene Panel.

A. Alzahrani, M. Abouelhoda, H. Al-Hindi, 2020, The Journal of clinical endocrinology and metabolism.

TERT promoter mutations in thyroid cancer: a report from a Middle Eastern population.

M. Xing, A. Alzahrani, H. Al-Hindi, 2015, Endocrine-related cancer.

Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer

Yufei Shi, A. Alzahrani, H. Al-Hindi, 2016, Journal of Translational Medicine.

S100A4 (Mts1) gene overexpression is associated with invasion and metastasis of papillary thyroid carcinoma

M. Zou, Y. Shi, N. Farid, 2005, British Journal of Cancer.

Novel homozygous mutation in DSP causing skin fragility–woolly hair syndrome: report of a large family and review of the desmoplakin‐related phenotypes

O. Khalifa, H. Al-Hindi, S. Wakil, 2011, Clinical genetics.

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder

Olfat Al-Harazi, N. Kaya, D. Çolak, 2014, Journal of Medical Genetics.

Controversy on the management of patients carrying RET p.V804M mutation

A. Alzahrani, H. Al-Hindi, Meshael M. Alswailem, 2021, Endocrine.

Vici syndrome associated with unilateral lung hypoplasia and myopathy

M. Al-Owain, H. Al-Hindi, H. Humaidan, 2010, American journal of medical genetics. Part A.

Familial paraganglioma due to a novel SDHB mutation: familial phenotypic heterogeneity and a potentially novel manifestation

A. Alzahrani, H. Al-Hindi, Meshael M. Alswailem, 2019, International Journal of Endocrine Oncology.

Unusual cause of ectopic secretion of adrenocorticotropic hormone: Cushing syndrome attributable to small cell prostate cancer.

A. Alzahrani, H. Al-Hindi, Omalkhaire M. Alshaikh, 2010, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Femoral Pathological Fracture as the First Clinical Manifestation of Papillary Thyroid Carcinoma in a Primigravida

A. Abu-Zaid, H. Al-Hindi, A. Azzam, 2013, Case reports in pathology.

Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy

J. Casanova, N. Kaya, A. Puel, 2010, Clinical & developmental immunology.

Appendiceal spirochetosis: a light and electron microscope study of two cases.

A. Haleem, H. Al-Hindi, H. Al Husseini, 2003, Annals of Saudi medicine.

Clinicopathologic and genomic characterizations of brain metastases using a comprehensive genomic panel

H. Robinson, Duna H. Barakeh, M. Abedalthagafi, 2022, Frontiers in Medicine.

Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome

B. Meyer, D. Monies, D. Jaroudi, 2014, Neuromuscular Disorders.

Central Nervous System Brucellosis Granuloma and White Matter Disease in Immunocompromised Patient

H. Al-Hindi, F. Al-Ajlan, M. Alqwaifly, 2017, Emerging infectious diseases.

Mature (Benign) Cystic Retroperitoneal Teratoma Involving the Left Adrenal Gland in a 22-Year-Old Male: A Case Report and Literature Review

A. Abu-Zaid, H. Al-Hindi, A. Azzam, 2013, Case reports in oncological medicine.

Response of medulloblastoma cells to vincristine and lomustine: role of TRKC, CTNNB1 and STK15.

A. Aboussekhra, Y. Khafaga, Z. Shinwari, 2011, Anticancer research.

One genotype, many phenotypes: SDHB p.R90X mutation-associated paragangliomas

A. Alzahrani, H. Al-Hindi, Yosra Moria, 2020, Endocrine.

Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.

N. Kaya, D. Çolak, Y. Lakmache, 2013, American journal of human genetics.

Single Point Mutations in Pediatric Differentiated Thyroid Cancer.

Yufei Shi, A. Alzahrani, H. Al-Hindi, 2017, Thyroid : official journal of the American Thyroid Association.

A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome

N. Kaya, D. Çolak, E. Alshail, 2023, Frontiers in Oncology.

Isolated renal hydatid disease in a non-endemic country: a single centre experience.

H. Al-Hindi, R. Seyam, A. Mokhtar, 2012, Canadian Urological Association journal = Journal de l'Association des urologues du Canada.

Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma

M. Dasouki, A. Alzahrani, M. Abouelhoda, 2019, Oncotarget.

A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype

Mohammed I. Alghamdi, M. Zou, N. Kaya, 2011, Clinical endocrinology.

MYH1 is a candidate gene for recurrent rhabdomyolysis in humans

F. Alkuraya, S. Arold, H. Al-Hindi, 2021, American journal of medical genetics. Part A.

Clinical and biochemical features associated with BCS1L mutation

Robert W. Taylor, N. Kaya, D. Çolak, 2013, Journal of Inherited Metabolic Disease.

Juvenile Hyaline Fibromatosis: Morphologic, Immunohistochemical, and Ultrastructural Study of Three Siblings

A. Haleem, H. Al-Hindi, A. Ajlan, 2002, The American Journal of dermatopathology.

Juvenile Hyaline Fibromatosis

A. Haleem, H. Al-Hindi, A. Ajlan, 2002 .

January 1997 ‐ 7 Year Old Girl with Seizures

B. Subach, H. Al-Hindi, Ronald L. Hamilton, 1997, Brain pathology.

Cauda equina syndrome as the initial presenting clinical feature of medulloblastoma: a case report

Faisal Al-Otaibi, H. Al-Hindi, Amani Al Kofide, 2012, Journal of Medical Case Reports.

Surgical Outcome of Thyroid Nodules with Atypia of Undetermined Significance and Follicular Lesion of Undetermined Significance in Fine Needle Aspiration Biopsy

H. Al-Hindi, A. Agarwal, S. Najjar, 2017 .

Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer

A. Alzahrani, H. Al-Hindi, Yosra Moria, 2018, Endocrine.

Large‐scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype

H. Al-Hindi, Abdulaziz Alsemari, 2015, Clinical case reports.

Clinical and genetic features of Calpainopathies in Saudi Arabia - a descriptive cross-sectional study.

H. Al-Hindi, E. Cupler, I. Alhomud, 2021, European review for medical and pharmacological sciences.

Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and Outcome

A. Alzahrani, H. Al-Hindi, Yosra Moria, 2018, The Journal of clinical endocrinology and metabolism.

Analysis of ALK, IDH1, IDH2 and MMP8 somatic mutations in differentiated thyroid cancers

A. Alzahrani, H. Al-Hindi, Ebtesam Qasem, 2021, Molecular and clinical oncology.

Absence of somatic mutations of the mTOR gene in differentiated thyroid cancer

A. Alzahrani, H. Al-Hindi, Z. Hassan, 2015, Meta gene.

GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancer

A. Alzahrani, H. Al-Hindi, Ebtesam Qasem, 2019, Oncotarget.

Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer

Yufei Shi, A. Alzahrani, H. Al-Hindi, 2016, Journal of Translational Medicine.

Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant

A. Alzahrani, H. Al-Hindi, A. Aljomaiah, 2022, Frontiers in Genetics.

Single nucleotide polymorphisms in matrix metalloproteinase 2 (MMP2) enhance BRAFV600E mutation-mediated oncogenicity and invasiveness of papillary thyroid cancer cells.

P. Manogaran, A. Alzahrani, M. Al-Ansari, 2021, Endocrine-related cancer.

Thyroid Cancer, Neuroendocrine Tumor, Adrenal Adenoma, and Other Tumors in a Patient With a Germline PMS1 Mutation

A. Alzahrani, H. Al-Hindi, A. K. Murugan, 2023, Journal of the Endocrine Society.

The impact of thyroid imaging reporting and data system on the management of Bethesda III thyroid nodules

S. Al-Sobhi, H. Al-Hindi, Saad M. Alqahtani, 2022, Journal of Taibah University Medical Sciences.

Fumarate hydratase is a novel gene for familial non-medullary thyroid cancer.

A. Alzahrani, H. Al-Hindi, Meshael M. Alswailem, 2022, The Journal of clinical endocrinology and metabolism.