[Fibroblast growth factors, their receptors and congenital diseases]

Clinical segmentation in 22q11.2 deletion syndrome: Cognitive impairments and additional genetic load.

Journal of psychiatric research·2024

Segway® related injuries in Vienna: report from the Lorenz Böhler Trauma Centre.

European journal of trauma and emergency surgery : official publication of the European Trauma Society·2015

Clinical presentations of 23 half-siblings from a mosaic neurofibromatosis type 1 sperm donor.

Clinical genetics·2015

[Radiological evaluation of k-wire osteosynthesis, in comparison to fixed-angle-plate osteosynthesis, in patients aged 80 years or more with distal radius fractures].

Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V...·2014

Gonosomal mosaicism for an NF1 deletion in a sperm donor: evidence of the need for coordinated, long-term communication of health information among relevant parties.

Human reproduction (Oxford, England)·2012

FGFR3 mutations and the skin: report of a patient with a FGFR3 gene mutation, acanthosis nigricans, hypochondroplasia and hyperinsulinemia and review of the literature.

Dermatology (Basel, Switzerland)·2010

[Myelin oligodendrocyte glycoprotein antibody-associated disease].

Ugeskrift for laeger·2026

[Clinical pharmacogenetics and the use of biobanks].

Ugeskrift for laeger·2026

[Cutaneous myiasis].

Ugeskrift for laeger·2026

[When radiology does not rule out intracranial hypertension].

Ugeskrift for laeger·2026

[Intracranial hypotension].

Ugeskrift for laeger·2026

[Large macrocystic lymphatic malformation in a newborn].

Ugeskrift for laeger·2026

SMURF1 alleviates preeclampsia by suppressing ferroptosis in trophoblast cells via mediating ubiquitination of FLT1.

Cellular signalling·2026

Risk of monozygotic twinning associated with different blastocyst transfer strategies in single embryo transfer cycles.

European journal of obstetrics, gynecology, and reproductive biology·2026

Singleton freemartinism in cattle: A structured narrative review and historical case reappraisal.

Theriogenology·2026

The Building and Application of a Machine Learning Model on Predicting Euploid Blastocysts in IVF Treatments Without PGT-A.

Reproductive sciences (Thousand Oaks, Calif.)·2026

A context-specific evaluation of polygenic embryo screening in best-prognosis preimplantation genetic testing cycles.

Human reproduction open·2026

Familial 46,XY disorder of sex development due to a novel CYB5A variant: a rare cause of isolated 17,20-lyase deficiency.

JCEM case reports·2026

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Clinical segmentation in 22q11.2 deletion syndrome: Cognitive impairments and additional genetic load.

Segway® related injuries in Vienna: report from the Lorenz Böhler Trauma Centre.

Clinical presentations of 23 half-siblings from a mosaic neurofibromatosis type 1 sperm donor.

[Radiological evaluation of k-wire osteosynthesis, in comparison to fixed-angle-plate osteosynthesis, in patients aged 80 years or more with distal radius fractures].

Gonosomal mosaicism for an NF1 deletion in a sperm donor: evidence of the need for coordinated, long-term communication of health information among relevant parties.

FGFR3 mutations and the skin: report of a patient with a FGFR3 gene mutation, acanthosis nigricans, hypochondroplasia and hyperinsulinemia and review of the literature.

[Myelin oligodendrocyte glycoprotein antibody-associated disease].

[Clinical pharmacogenetics and the use of biobanks].

[Cutaneous myiasis].

[When radiology does not rule out intracranial hypertension].

[Intracranial hypotension].

[Large macrocystic lymphatic malformation in a newborn].

SMURF1 alleviates preeclampsia by suppressing ferroptosis in trophoblast cells via mediating ubiquitination of FLT1.

Risk of monozygotic twinning associated with different blastocyst transfer strategies in single embryo transfer cycles.

Singleton freemartinism in cattle: A structured narrative review and historical case reappraisal.

The Building and Application of a Machine Learning Model on Predicting Euploid Blastocysts in IVF Treatments Without PGT-A.

A context-specific evaluation of polygenic embryo screening in best-prognosis preimplantation genetic testing cycles.

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