abnormalies < abnormalities < abnormality

Facettes : Author.f AffPays.f AffOrg.f AffRegion.f AffVille.f

List of bibliographic references

Number of relevant bibliographic references: 243.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000217 (1994)	G. Borroni [Italie] ; D. Larizza [Italie] ; G. Vignati [Italie] ; C. Zaccone [Italie] ; R. Zanetta [Italie] ; G. P. Vignoli [Italie] ; V. Brazzelli [Italie] ; C. Bobba [Italie] ; G. Rabbiosi [Italie]	The dermatological spectrum of Turner syndrome
000242 (1989)	Shinichi Miyabara [Japon] ; Hajime Sugihara [Japon] ; Norifumi Maehara [Japon] ; Hideaki Shouno [Japon] ; Hakaru Tasaki [Japon] ; Keiji Yoshida [Japon] ; Nakamichi Saito [Japon] ; Fumiyoshi Kayama [Japon] ; Satoshi Ibara [Japon] ; Kaoru Suzumori [Japon]	Significance of cardiovascular malformations in cystic hygroma: A new interpretation of the pathogenesis
000259 (1998)	Oliviero Sacco [Italie] ; Bruno Fregonese [Italie] ; Carla E. Marino [Italie] ; Girolamo Mattioli [Italie] ; Claudio Gambini [Italie] ; Giovanni A. Rossi [Italie]	Yellow nail syndrome and bilateral cystic lung disease
000261 (1996)	Betsy D. Carlton ; Jean-Claude Aubrun [France] ; Glenn S. Simon	Effects of Coumarin Following Perinatal and Chronic Exposure in Sprague–Dawley Rats and CD-1 Mice
000339 (1983)	Claude S. Dahlberg [États-Unis] ; Claude S. Borer [États-Unis] ; Kermit L. Newcomer [États-Unis] ; Wilfrido R. Yutuc [États-Unis]	Autosomal or X‐linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy
000376 (2003)	Nataša Mar Un Varda [Slovénie] ; N. Kokalj Voka [Slovénie] ; Z. Kani [Slovénie] ; K. Bra I [Slovénie] ; A. Erjavec [Slovénie] ; B. Zagradišnik [Slovénie] ; A. Gregori [Slovénie]	Early renal insufficiency in a neonate with de novo partial trisomy of chromosome 10q
000494 (2002)	Brigitte Granel [France] ; Jacques Serratrice [France] ; Jean Michel Bartoli [France] ; Patrick Disdier [France] ; Philippe Piquet [France] ; Pierre-Jean Weiller [France]	Bilateral Iliac Vein Thrombosis After Seat Belt-Related Trauma Revealing Hypoplasia of the Inferior Vena Cava
000560 (2002)	Caroline Thaung [Royaume-Uni] ; Katrine West [Royaume-Uni] ; Brian J. Clark [Royaume-Uni] ; Lisa Mckie [Royaume-Uni] ; Joanne E. Morgan [Royaume-Uni] ; Karen Arnold [Royaume-Uni] ; Patrick M. Nolan [Royaume-Uni] ; Jo Peters [Royaume-Uni] ; A. Jackie Hunter [Royaume-Uni] ; Steve D. M. Brown [Royaume-Uni] ; Ian J. Jackson [Royaume-Uni] ; Sally H. Cross [Royaume-Uni]	Novel ENU-induced eye mutations in the mouse: models for human eye disease
000637 (1979)	I. Kondo ; H. Hamaguchi ; A. Matsuura ; H. Nakajima ; A. Koyama ; H. Takita	A case of Turner's syndrome with familial balanced translocation t(1;2)(q32;q21)mat.
000690 (1994)	Deborah L. Keefe [États-Unis] ; Nancy Roistacher [États-Unis] ; Mary Kathryn Pierri [États-Unis]	Evaluation of Suspected Deep Venous Thrombosis in Oncologic Patients
000732 (1999)	Mark D. Harrison ; Charles T. Dameron	Molecular mechanisms of copper metabolism and the role of the Menkes disease protein
000784 (1989)	David Chitayat [Canada] ; David Kalousek [Canada] ; J. Stephen Bamforth [Canada]	Lymphatic abnormalities in fetuses with posterior cervical cystic hygroma
000790 (2013)	Dima R. Ezmigna [États-Unis] ; Wayne J. Morgan [États-Unis] ; Marlys H. Witte [États-Unis] ; Mark A. Brown [États-Unis]	Lymphoscintigraphy in plastic bronchitis, A pediatric case report
000807 (2000)	Barbara R. Migeon [États-Unis] ; Margareet Ausems [Pays-Bas] ; Jacques Giltay [Pays-Bas] ; Camille Hasley-Royster [États-Unis] ; Ethan Kazi [États-Unis] ; Thomas J. Lydon [États-Unis] ; John J. M. Engelen [Pays-Bas] ; Gerald V. Raymond [États-Unis]	Severe phenotypes associated with inactive ring X chromosomes
000A08 (1989)	Tsuyoshi Sato [Japon] ; Yasuhiko Morita [Japon] ; Kazunori Kawano [Japon] ; Shigeaki Suenaga [Japon] ; Akito Tomomura [Japon] ; Takenori Noikura [Japon]	Clinical evaluation of lymphoscintigraphy of the head and neck
000A96 (1981)	Soichiro Miura [Japon] ; Hitoshi Asakura [Japon] ; Masaharu Tsuchiya [Japon]	Lymphatic Abnormalities in Protein-Losing Gastropathy, Especially in Ménétrier's Disease
000C57 (1966)	D. G. Harnden	Sex chromosome abnormalities in children
000D79 (1965)	Joseph J. Bookstein ; Arthur B. French ; H. Marvin Pollard	Protein-losing gastroenteropathy: Concepts derived from lymphangiography
000D80 (2007)	R. Shayan [Australie] ; T. Karnesis [Australie] ; K. Paavonen [Australie] ; M. G. Achen [Australie] ; G. I. Taylor [Australie] ; S. A. Stacker [Australie]	PR07A SYSTEM FOR QUANTIFYING LYMPHATIC VESSEL ABNORMALITIES IN LYMPHEDEMA MODELS, AND LOCO‐SYSTEMIC EFFECTS OF PRO‐LYMPHATIC TUMOR GROWTH FACTORS
000F62 (1996)	Mary Ella M. Pierpont [États-Unis]	Genetic etiology of cardiac syndromes
000F96 (2005)	N. J. Hilliard [États-Unis] ; Y. Hammers [États-Unis] ; E. Martin [États-Unis] ; P. Howard [États-Unis] ; E. M. Omura [États-Unis] ; D. R. Kelly [États-Unis]	Cutaneous Manifestations of Juvenile Hyaline Fibromatosis

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Istex/Curation

HfdIndexSelect -h $EXPLOR_AREA/Data/Istex/Curation/AbsEn.i -k "abnormalities" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Istex/Curation/AbsEn.i  \
                -Sk "abnormalities" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Istex/Curation/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
   |flux=    Istex
   |étape=   Curation
   |type=    indexItem
   |index=    AbsEn.i
   |clé=    abnormalities
}}

---

This area was generated with Dilib version V0.6.31. Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024