Search Results - "Rampling, D."

Author index to Volume 85.

Source: British Journal of Cancer. 12/15/2001, Vol. 85 Issue 12, p2026. 9p.

Synchronous multiple primary malignancies or transdifferentiation?—A diagnostic challenge in a case of Xeroderma pigmentosum.

Authors: Kanna, Sandhyarani M. Sandeepa, Supriya Mukund, K. N. et al.

Source: Indian Journal of Pathology & Microbiology. Jul-Sep2025, Vol. 68 Issue 3, p616-619. 4p.

Religious and Spiritual Dimensions of Pro-Ana Discourse on X: A Linguistic Analysis for Counseling Practice.

Authors: Elrod, Krisy Trifonopoulos, Angeliki

Source: Behavioral Sciences (2076-328X). Dec2025, Vol. 15 Issue 12, p1626. 13p.

Constructing Moral Selves Through Food: A Qualitative Study of Orthorexic Eating Practices in the UK.

Authors: Tragantzopoulou, Panagiota Mitrofanova, Elina Giannouli, Vaitsa

Source: Behavioral Sciences (2076-328X). Jun2026, Vol. 16 Issue 6, p997. 26p.

Sensitive detection of minimal residual disease and immunotherapy targets by multi-modal bone marrow analysis in high-risk neuroblastoma – a multi-center study.

Authors: Gelineau, Nina U. Bozsaky, Eva van Zogchel, Lieke M. J. et al.

Source: Journal of Experimental & Clinical Cancer Research (17569966). 8/2/2025, Vol. 44 Issue 1, p1-16. 16p.

ATRX mutations mediate an immunogenic phenotype and macrophage infiltration in neuroblastoma.

Authors: Lorenzi F Jostes S Gao Q et al.

Source: Cancer letters [Cancer Lett] 2025 Mar 31; Vol. 613, pp. 217495. Date of Electronic Publication: 2025 Jan 30.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Science Ireland Country of Publication: Ireland NLM ID: 7600053 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-7980 (Electronic) Linking ISSN: 03043835 NLM ISO Abbreviation: Cancer Lett Subsets: MEDLINE

Why and when are activity scores and advanced ultrasound techniques needed in inflammatory bowel disease (IBD)?

Authors: Jenssen, Christian Petersen, Frauke Höpfner, Michael et al.

Source: Medical Ultrasonography. Mar2026, Vol. 28 Issue 1, p58-69. 12p.

The Evolving Role of Cine MRI in Crohn's Disease: From Functional Motility Analysis to Precision Management: A Review of the Last 10 Years.

Authors: Alyami, Ali S.¹ (AUTHOR)

Source: Diagnostics (2075-4418). Dec2025, Vol. 15 Issue 23, p3078. 20p.

Analysis of Bone Phenotype Differences in MEN1-Related and Sporadic Primary Hyperparathyroidism Using 3D-DXA.

Authors: Eremkina, Anna K. Pylina, Svetlana V. Elfimova, Alina R. et al.

Source: Journal of Clinical Medicine. Nov2024, Vol. 13 Issue 21, p6382. 16p.

Infantile hemangiomas: a dermatologist's perspective.

Authors: Sharma, Apoorva Gupta, Manavi Mahajan, Rahul

Source: European Journal of Pediatrics. Oct2024, Vol. 183 Issue 10, p4159-4168. 10p.

Antroduodenal manometry findings in children with suspected pediatric intestinal pseudo‐obstruction.

Authors: Gulliksson, Gullik Nyström, Niklas Danielson, Johan et al.

Source: Neurogastroenterology & Motility. Sep2024, Vol. 36 Issue 9, p1-8. 8p.

Diagnosis and Management of Functional Pancreatic Neuroendocrine Tumors in Children—A Systematic Review.

Authors: Keretić, Dorotea Bašković, Marko

Source: Diagnostics (2075-4418). Sep2025, Vol. 15 Issue 17, p2176. 32p.

Fetal rhabdomyoma in a Thoroughbred filly.

Authors: Rapezzano, Giulia Foote, Alastair Petrini, Filippo et al.

Source: Veterinary Medicine & Science. Jul2024, Vol. 10 Issue 4, p1-6. 6p.

Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review.

Authors: Zhuang, Jianlong Luo, Qi Xie, Meihua et al.

Source: Molecular Genetics & Genomic Medicine. Mar2023, Vol. 11 Issue 3, p1-6. 6p.

Does the gene matter? Genotype‐phenotype and genotype‐outcome associations in congenital melanocytic naevi.

Authors: Polubothu, S. McGuire, N. Al‐Olabi, L. et al.

Source: The British journal of dermatology Feb2020; Vol. 182 (2).

Journal Info: Publisher: Oxford University Press / USA ISSN: 0007-0963

Most appropriate surgical approach in children with Wilms tumour, risk of kidney disease, and related considerations.

Authors: Spreafico, Filippo Biasoni, Davide Montini, Giovanni

Source: Pediatric Nephrology. Apr2024, Vol. 39 Issue 4, p1019-1022. 4p.

A Potential Prognostic Gene Signature Associated with p53-Dependent NTRK1 Activation and Increased Survival of Neuroblastoma Patients.

Authors: Currie, David Wong, Nicole Zane, Isabelle et al.

Source: Cancers. Feb2024, Vol. 16 Issue 4, p722. 19p.

Profiling the Resident and Infiltrating Monocyte/Macrophages during Rejection following Kidney Transplantation.

Authors: Wang, Jie Luo, Peiling Zhao, Jingjie et al.

Source: Journal of Immunology Research. 9/21/2020, p1-14. 14p. 5 Graphs.

The population frequency of predicted pathogenic genetic variants in commonly affected CAKUT genes in the general population.

Authors: Huang M Savige J

Source: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2026 May 16. Date of Electronic Publication: 2026 May 16.

Publication Type: Journal Article

Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-198X (Electronic) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE

A novel NSDHL variant in CHILD syndrome with gastrointestinal manifestations and localized skin involvement.

Authors: Tan, Ene‐Choo Chia, Shi Yun Rafi'ee, Khadijah et al.

Source: Molecular Genetics & Genomic Medicine. Jan2022, Vol. 10 Issue 1, p1-8. 8p.