[Polysyndactyly, short limbs, and genital malformations--a new syndrome?]

[Bladder cancer screening with urine-based tumour markers - occupational medical experience].

Aktuelle Urologie·2011

Development of a porcine animal model for urethral stricture repair using autologous urothelial cells.

Journal of pediatric urology·2011

[Bioartificial urothelium generated from bladder washings. A future therapeutic option for reconstructive surgery].

Der Urologe. Ausg. A·2008

A novel polyarginine containing Smac peptide conjugate that mediates cell death in tumor and healthy cells.

Medicinal chemistry (Shariqah (United Arab Emirates))·2008

[Tissue engineering and stem cell research in urology for a reconstructive or regenerative treatment approach].

Der Urologe. Ausg. A·2007

[Value of stem cell therapy for the treatment of stress incontinence. Current status and perspectives].

Der Urologe. Ausg. A·2007

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

Zeitschrift fur Kinderheilkunde·1975

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Incidence of malignant tumors in childhood (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

Zeitschrift fur Kinderheilkunde·1975

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

Zeitschrift fur Kinderheilkunde·1975

Retrospective Analysis of Paenibacillus urinalis Cultures Primarily Obtained from Sterile Sites in a Pediatric Population from Turkey.

Microorganisms·2026

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

Genes·2026

Never Say Never: Presumed Inherited Factor VII Deficiency Lies in Wait for 17 Years.

Cureus·2026

Simultaneous Bilateral Tibial Tubercle Avulsion Fractures Complicated by Compartment Syndrome in an Adolescent With Osteogenesis Imperfecta: A Case Report.

Case reports in orthopedics·2026

Facial nerve schwannoma of the accessory parotid gland region in a child managed through a transoral approach.

BMJ case reports·2026

A Case of Pemphigus Herpetiformis in a 10-Year-Old Child.

Clinical, cosmetic and investigational dermatology·2026

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[Polysyndactyly, short limbs, and genital malformations--a new syndrome?]

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[Bladder cancer screening with urine-based tumour markers - occupational medical experience].

Development of a porcine animal model for urethral stricture repair using autologous urothelial cells.

[Bioartificial urothelium generated from bladder washings. A future therapeutic option for reconstructive surgery].

A novel polyarginine containing Smac peptide conjugate that mediates cell death in tumor and healthy cells.

[Tissue engineering and stem cell research in urology for a reconstructive or regenerative treatment approach].

[Value of stem cell therapy for the treatment of stress incontinence. Current status and perspectives].

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

[Incidence of malignant tumors in childhood (author's transl)].

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

Retrospective Analysis of Paenibacillus urinalis Cultures Primarily Obtained from Sterile Sites in a Pediatric Population from Turkey.

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

Never Say Never: Presumed Inherited Factor VII Deficiency Lies in Wait for 17 Years.

Simultaneous Bilateral Tibial Tubercle Avulsion Fractures Complicated by Compartment Syndrome in an Adolescent With Osteogenesis Imperfecta: A Case Report.

Facial nerve schwannoma of the accessory parotid gland region in a child managed through a transoral approach.

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