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Hartmut P. H. Neumann

Nephrologe

Name	Hartmut P. H. Neumann
Ort	Deutschland
Akademischer Grad bzw. Titel	Prof. Dr. med.
Beruf	Nephrologe (charakteristischer Beruf)
Variante	H. P. H. Neumann
Datensatztyp	Person
GND-Nummer	124439624
Datensatz-ID	124439624
Beteiligt an alle anzeigen Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment Clinical decision making in small non-functioning VHL-related incidentalomas Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study Comparison of pheochromocytoma-specific morbidity and mortality among adults with bilateral pheochromocytomas undergoing total adrenalectomy vs cortical-sparing adrenalectomy Growth characteristics and therapeutic decision markers in von Hippel Lindau disease patients with renal cell carcinoma Max Schottelius: Pioneer in Pheochromocytoma Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis Characteristics of intracranial aneurysms in the else Kröner-Fresenius registry of autosomal dominant polycystic kidney disease Growth kinetics in Von Hippel-Lindau-associated renal cell carcinoma Phaeochromocytomák, paragangliomák, glomustumorok és társuló betegségek : von Hippel-Lindau-szindróma, multiplex endokin neoplasia 2-es típusa, neurofibromatosis 1-es típusa, öröklődő paraganglioma szindrómák ; tájékoztató betegek és hozzátartozóik részére Pheochromocytoma – where are we? Where should we go? A medical and scientific odyssey : Review Die von-Hippel-Lindau-Erkrankung : ein Leitfaden für Betroffene und Ärzte VHL - die von-Hippel-Lindau-Krankheit : ein Leitfaden für Betroffene und Ärzte Die Von-Hippel-Lindau-Erkrankung : Leitfaden für Patienten und Ärzte Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect

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Katalog der Deutschen Nationalbibliothek

Hartmut P. H. Neumann

Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease

Screening and surveillance recommendations for central nervous system hemangioblastomas in pediatric patients with Von Hippel-Lindau disease

Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment

Clinical decision making in small non-functioning VHL-related incidentalomas

Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment

Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study

Comparison of pheochromocytoma-specific morbidity and mortality among adults with bilateral pheochromocytomas undergoing total adrenalectomy vs cortical-sparing adrenalectomy

Growth characteristics and therapeutic decision markers in von Hippel Lindau disease patients with renal cell carcinoma

Max Schottelius: Pioneer in Pheochromocytoma

Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma

Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis

Characteristics of intracranial aneurysms in the else Kröner-Fresenius registry of autosomal dominant polycystic kidney disease

Growth kinetics in Von Hippel-Lindau-associated renal cell carcinoma

Phaeochromocytomák, paragangliomák, glomustumorok és társuló betegségek : von Hippel-Lindau-szindróma, multiplex endokin neoplasia 2-es típusa, neurofibromatosis 1-es típusa, öröklődő paraganglioma szindrómák ; tájékoztató betegek és hozzátartozóik részére

Pheochromocytoma – where are we? Where should we go? A medical and scientific odyssey : Review

Die von-Hippel-Lindau-Erkrankung : ein Leitfaden für Betroffene und Ärzte

VHL - die von-Hippel-Lindau-Krankheit : ein Leitfaden für Betroffene und Ärzte

Die Von-Hippel-Lindau-Erkrankung : Leitfaden für Patienten und Ärzte

Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect