Von Hippel-Lindau disease (VHLD)

Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and t...
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Autor*in:	Jorge Luis González Jara [verfasserIn]

Format:	E-Artikel
Sprache:	Spanisch

Erschienen:	2009

Schlagwörter:	enfermedad de hippel-lindau/historia estudios de seguimiento

Übergeordnetes Werk:	In: Acta Médica del Centro - Editorial Ciencias Médicas, 2021, 3(2009), 3, Seite 60-66
Übergeordnetes Werk:	volume:3 ; year:2009 ; number:3 ; pages:60-66

Links:	Link aufrufen Link aufrufen Journal toc

Katalog-ID:	DOAJ027021734

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spelling	(DE-627)DOAJ027021734 (DE-599)DOAJa1a35b52b5a54058bc9e2a84977df75c DE-627 ger DE-627 rakwb spa Jorge Luis González Jara verfasserin aut Von Hippel-Lindau disease (VHLD) 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations. enfermedad de hippel-lindau/historia estudios de seguimiento Medicine R In Acta Médica del Centro Editorial Ciencias Médicas, 2021 3(2009), 3, Seite 60-66 (DE-627)1676953329 27097927 nnns volume:3 year:2009 number:3 pages:60-66 https://doaj.org/article/a1a35b52b5a54058bc9e2a84977df75c kostenfrei http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/465 kostenfrei https://doaj.org/toc/2709-7927 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2009 3 60-66
allfields_unstemmed	(DE-627)DOAJ027021734 (DE-599)DOAJa1a35b52b5a54058bc9e2a84977df75c DE-627 ger DE-627 rakwb spa Jorge Luis González Jara verfasserin aut Von Hippel-Lindau disease (VHLD) 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations. enfermedad de hippel-lindau/historia estudios de seguimiento Medicine R In Acta Médica del Centro Editorial Ciencias Médicas, 2021 3(2009), 3, Seite 60-66 (DE-627)1676953329 27097927 nnns volume:3 year:2009 number:3 pages:60-66 https://doaj.org/article/a1a35b52b5a54058bc9e2a84977df75c kostenfrei http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/465 kostenfrei https://doaj.org/toc/2709-7927 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2009 3 60-66
allfieldsGer	(DE-627)DOAJ027021734 (DE-599)DOAJa1a35b52b5a54058bc9e2a84977df75c DE-627 ger DE-627 rakwb spa Jorge Luis González Jara verfasserin aut Von Hippel-Lindau disease (VHLD) 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations. enfermedad de hippel-lindau/historia estudios de seguimiento Medicine R In Acta Médica del Centro Editorial Ciencias Médicas, 2021 3(2009), 3, Seite 60-66 (DE-627)1676953329 27097927 nnns volume:3 year:2009 number:3 pages:60-66 https://doaj.org/article/a1a35b52b5a54058bc9e2a84977df75c kostenfrei http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/465 kostenfrei https://doaj.org/toc/2709-7927 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2009 3 60-66
allfieldsSound	(DE-627)DOAJ027021734 (DE-599)DOAJa1a35b52b5a54058bc9e2a84977df75c DE-627 ger DE-627 rakwb spa Jorge Luis González Jara verfasserin aut Von Hippel-Lindau disease (VHLD) 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations. enfermedad de hippel-lindau/historia estudios de seguimiento Medicine R In Acta Médica del Centro Editorial Ciencias Médicas, 2021 3(2009), 3, Seite 60-66 (DE-627)1676953329 27097927 nnns volume:3 year:2009 number:3 pages:60-66 https://doaj.org/article/a1a35b52b5a54058bc9e2a84977df75c kostenfrei http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/465 kostenfrei https://doaj.org/toc/2709-7927 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 3 2009 3 60-66
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author	Jorge Luis González Jara
spellingShingle	Jorge Luis González Jara misc enfermedad de hippel-lindau/historia misc estudios de seguimiento misc Medicine misc R Von Hippel-Lindau disease (VHLD)
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topic_title	Von Hippel-Lindau disease (VHLD) enfermedad de hippel-lindau/historia estudios de seguimiento
topic	misc enfermedad de hippel-lindau/historia misc estudios de seguimiento misc Medicine misc R
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title	Von Hippel-Lindau disease (VHLD)
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title_full	Von Hippel-Lindau disease (VHLD)
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title_sort	von hippel-lindau disease (vhld)
title_auth	Von Hippel-Lindau disease (VHLD)
abstract	Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations.
abstractGer	Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations.
abstract_unstemmed	Von Hippel-Lindau disease is one the 7000 known hereditary disorder. It is named after Dr. Eugen von Hippel; a German ophthalmologist who was the first to described the ocular angiomas in 1895. Equally, Dr. Arvid Lindau, a Swedish pathologist, begins the study of the angiomas in the cerebellum and the spinal cord marrow in 1926. His description includes a systematic recompilation of all the cases published up to that time, including those described by von Hippel, but adding also the alterations in other abdominal organs. It is an autosomal dominant neoplasia syndrome caused by the deletion or mutation of the tumor suppressor gene of the 3p25 chromosome, characterized by the presence of benign and malignant tumors affecting several organs and systems such as: the central nervous system, the pancreas, the adrenal glands and the paranodes. In general, the disease is hereditary; but the health problems affecting the patients can be so varied that the common cause may not be identified. Besides, the appearance and severity of the disease have a great variation, and within the same family there are individuals slightly affected while others present more serious manifestations.
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title_short	Von Hippel-Lindau disease (VHLD)
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