The vulnerability of retina neuroblast after metabolic errors

Cartilage-flow phenomenon and evidence for it in perichondrial grafting.

Archives of orthopaedic and trauma surgery·1997

Variability of femoral muscle attachments.

Journal of biomechanics·1996

[New kinds of 3-dimensional atlases of the anatomy and function of the human body].

Zeitschrift fur arztliche Fortbildung·1995

[Angio-architecture of the colon in Crohn disease and ulcerative colitis. Light microscopy and scanning electron microscopy studies with reference to the morphology of the healthy large intestine].

Langenbecks Archiv fur Chirurgie·1995

Anal endosonography in healthy subjects and patients with idiopathic fecal incontinence.

Diseases of the colon and rectum·1994

[Thermal side effects after use of the pulsed IR laser on meniscus and bone tissue].

Unfallchirurgie·1994

Evaluation of morphological and dimensional characteristics of the nasopalatine canal in patients with impacted teeth in the anterior maxilla: a retrospective study.

Folia morphologica·2026

The aberrant right subclavian artery and non-recurrent laryngeal nerve: a cadaveric study.

Folia morphologica·2026

Ten concurrent anatomical variations in a single cadaver involving the muscular, vascular, and nervous systems.

Folia morphologica·2026

The complete anatomy of the superior cerebellar artery: a systematic review and meta-analysis with clinical implications.

Folia morphologica·2026

Three-dimensional computed tomography assessment of acromial morphology in Vietnamese patients undergoing arthroscopic surgery for subacromial impingement.

Folia morphologica·2026

Computed tomography angiographic examination of coronary sinus morphometry and spatial orientation: a guide for cardiac resynchronization therapy procedures.

Folia morphologica·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

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The vulnerability of retina neuroblast after metabolic errors

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Cartilage-flow phenomenon and evidence for it in perichondrial grafting.

Variability of femoral muscle attachments.

[New kinds of 3-dimensional atlases of the anatomy and function of the human body].

[Angio-architecture of the colon in Crohn disease and ulcerative colitis. Light microscopy and scanning electron microscopy studies with reference to the morphology of the healthy large intestine].

Anal endosonography in healthy subjects and patients with idiopathic fecal incontinence.

[Thermal side effects after use of the pulsed IR laser on meniscus and bone tissue].

Evaluation of morphological and dimensional characteristics of the nasopalatine canal in patients with impacted teeth in the anterior maxilla: a retrospective study.

The aberrant right subclavian artery and non-recurrent laryngeal nerve: a cadaveric study.

Ten concurrent anatomical variations in a single cadaver involving the muscular, vascular, and nervous systems.

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Three-dimensional computed tomography assessment of acromial morphology in Vietnamese patients undergoing arthroscopic surgery for subacromial impingement.

Computed tomography angiographic examination of coronary sinus morphometry and spatial orientation: a guide for cardiac resynchronization therapy procedures.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

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The vulnerability of retina neuroblast after metabolic errors

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