Search Results - "Fukami M"

Ten-Year Follow-Up of Visual Outcomes After Vitrectomy for Clinically Non-Tractional Diabetic Macular Edema.

Authors: Kumagai K Horie E Fukami M et al.

Source: Cureus [Cureus] 2025 Oct 27; Vol. 17 (10), pp. e95537. Date of Electronic Publication: 2025 Oct 27 (Print Publication: 2025).

Publication Type: Journal Article

Journal Info: Publisher: Cureus, Inc Country of Publication: United States NLM ID: 101596737 Publication Model: eCollection Cited Medium: Print ISSN: 2168-8184 (Print) Linking ISSN: 21688184 NLM ISO Abbreviation: Cureus Subsets: PubMed not MEDLINE

21‐Hydroxylase Deficient Congenital Adrenal Hyperplasia Due to Maternal Uniparental Isodisomy.

Authors: Kluge, Michelle L. Schema, Lynn Schroepfer, Katy et al.

Source: Case Reports in Endocrinology. 6/5/2026, Vol. 2026, p1-6. 6p.

De novo retrotransposon insertion into the FGFR1 gene in a boy with congenital hypogonadotropic hypogonadism: a case report.

Authors: Sawano K Nagasaki K Suzuki E et al.

Source: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2025 Jun 18; Vol. 16, pp. 1565316. Date of Electronic Publication: 2025 Jun 18 (Print Publication: 2025).

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE

Aromatase excess syndrome in children: insight on pathophysiology, clinical manifestation, and management.

Authors: Metwalley, Kotb Abbass Farghaly, Hekma Saad

Source: Journal of Rare Diseases. 2/12/2026, Vol. 5 Issue 1, p1-7. 7p.

The Expression of Placental 17β-Hydroxysteroid Dehydrogenase Genes Is Associated with the Elevation of Active Androgens and Estrogens in Pregnant Women, but Does Not Affect 11-Oxygenated C19 Steroids.

Authors: Yokohama, Yuko Watanabe, Yugo Nakajima, Ke-ichi et al.

Source: International Journal of Molecular Sciences. May2026, Vol. 27 Issue 10, p4290. 10p.

A maternal exon H splice-site variant leading to pseudohypoparathyroidism type 1B with broad methylation defects in GNAS-differentially methylated regions.

Authors: Urakawa T Huang H Nagai T et al.

Source: Clinical epigenetics [Clin Epigenetics] 2026 Mar 16; Vol. 18 (1). Date of Electronic Publication: 2026 Mar 16.

Publication Type: Journal Article

Journal Info: Publisher: Biomed Central Country of Publication: Germany NLM ID: 101516977 Publication Model: Electronic Cited Medium: Internet ISSN: 1868-7083 (Electronic) Linking ISSN: 18687075 NLM ISO Abbreviation: Clin Epigenetics Subsets: MEDLINE

A novel OPHN1 variant associated with cyclic strabismus but in the absence of OPHN1 syndrome.

Authors: Nishina S Kofuji S Matsubara K et al.

Source: Scientific reports [Sci Rep] 2026 Apr 24; Vol. 16 (1). Date of Electronic Publication: 2026 Apr 24.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE; In Process

Clinical features of syndromic microphthalmia in two novel RARB variants.

Authors: Koyanagi Y Morikawa-Anzai H Yoshida T et al.

Source: Human genome variation [Hum Genome Var] 2026 Apr 06; Vol. 13 (1). Date of Electronic Publication: 2026 Apr 06.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101652445 Publication Model: Electronic Cited Medium: Print ISSN: 2054-345X (Print) Linking ISSN: 2054345X NLM ISO Abbreviation: Hum Genome Var Subsets: PubMed not MEDLINE

Can interactive artificial intelligence be used for patient explanations of nuclear medicine examinations in Japanese?

Authors: Matsutomo N Fukami M Yamamoto T

Source: Annals of nuclear medicine [Ann Nucl Med] 2025 Aug; Vol. 39 (8), pp. 774-780. Date of Electronic Publication: 2025 Apr 16.

Publication Type: Journal Article

Journal Info: Publisher: Springer Japan Country of Publication: Japan NLM ID: 8913398 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1864-6433 (Electronic) Linking ISSN: 09147187 NLM ISO Abbreviation: Ann Nucl Med Subsets: MEDLINE

Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site.

Authors: Masubuchi H Urakawa T Kosaki R et al.

Source: Clinical epigenetics [Clin Epigenetics] 2026 Feb 03; Vol. 18 (1). Date of Electronic Publication: 2026 Feb 03.

Publication Type: Journal Article

Journal Info: Publisher: Biomed Central Country of Publication: Germany NLM ID: 101516977 Publication Model: Electronic Cited Medium: Internet ISSN: 1868-7083 (Electronic) Linking ISSN: 18687075 NLM ISO Abbreviation: Clin Epigenetics Subsets: MEDLINE

Association between miscarriage rates in modified natural ovulation cycles and hormone replacement cycles during frozen-thawed embryo transfer in three IVF JAPAN GROUP fertility clinics: a retrospective analysis.

Authors: Konishi, Haruhisa Matsumoto, Hiroshi Fujiwara, Sho et al.

Source: Middle East Fertility Society Journal. 3/7/2026, Vol. 31 Issue 1, p1-6. 6p.

Intrapapillary Hemorrhage With Adjacent Peripapillary Subretinal Hemorrhage and Reduced Blood Flow in the Optic Papillary Region Observed on Laser Speckle Flowgraphy.

Authors: Ikeda, Mizuki Oshitari, Toshiyuki Usui, Tomohiko et al.

Source: Case Reports in Ophthalmological Medicine. 2/24/2026, Vol. 2026, p1-6. 6p.

A long-term observational study on autoimmune pulmonary alveolar proteinosis revealed a sustained and generalized decrease in serum autoantibody levels.

Authors: Yamaguchi E Tanaka H Fujishiro E et al.

Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2026 Mar 11; Vol. 21 (1). Date of Electronic Publication: 2026 Mar 11.

Publication Type: Journal Article; Observational Study

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

Novel biallelic CDK9 variants are associated with retinal dystrophy without CHARGE-like malformation syndrome.

Authors: Nishina S Torii K Ishitani S et al.

Source: Journal of human genetics [J Hum Genet] 2026 Feb; Vol. 71 (2), pp. 97-103. Date of Electronic Publication: 2025 Sep 16.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-232X (Electronic) Linking ISSN: 14345161 NLM ISO Abbreviation: J Hum Genet Subsets: MEDLINE

Submicroscopic 16q24.2-q24.3 deletion in a family with nonsyndromic short stature.

Authors: Narita C Utsunomiya H Hamada J et al.

Source: Human genome variation [Hum Genome Var] 2026 Jan 26; Vol. 13 (1), pp. 2. Date of Electronic Publication: 2026 Jan 26.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101652445 Publication Model: Electronic Cited Medium: Print ISSN: 2054-345X (Print) Linking ISSN: 2054345X NLM ISO Abbreviation: Hum Genome Var Subsets: PubMed not MEDLINE

Clinical characteristics of pulmonary infections caused by Exophialadermatitidis.

Authors: Yonezawa T Nakamura A Onda Y et al.

Source: Respiratory investigation [Respir Investig] 2026 Jan; Vol. 64 (1), pp. 101355. Date of Electronic Publication: 2025 Dec 19.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101581124 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2212-5353 (Electronic) Linking ISSN: 22125345 NLM ISO Abbreviation: Respir Investig Subsets: MEDLINE

HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childhood Diabetes Registry: Clinical Insights and Prevalence Informed by Genetic and Functional Evaluation.

Authors: Pavithram, Aishwarya Johansson, Bente B. Tjora, Erling et al.

Source: International Journal of Molecular Sciences. Jun2026, Vol. 27 Issue 11, p5067. 20p.

Epigenetic Signatures in Hypospadias: Systematic Review.

Authors: Sharma, Jyoti Goel, Prabudh Yadav, Devendra Kumar et al.

Source: Journal of Indian Association of Pediatric Surgeons. May/Jun2026, Vol. 31 Issue 3, p418-426. 9p.

Molecular Age Estimation: Current Perspectives and Future Considerations.

Authors: Zaatar, Muriel Tahtouh Alghafri, Rashed Othman, Rima et al.

Source: International Journal of Molecular Sciences. Apr2026, Vol. 27 Issue 7, p3104. 18p.

Clinical Profile of Headache in Epilepsy: Experience from a Tertiary Center in South India.

Authors: Chaithra, S. P. Alamaddi, Vinusha Sannegowda, Raghavendra Bakki et al.

Source: APIK Journal of Internal Medicine. Apr-Jun2026, Vol. 14 Issue 2, p142-147. 6p.