Peter Robson < Peter S. Mortimer < Peter Salmon

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

List of bibliographic references

Number of relevant bibliographic references: 47.
[0-20] [0 - 20][0 - 47][20-40]

Ident.	Authors (with country if any)	Title
000001 (2017)	René H Gerling [Allemagne] ; Dominik Drees ; Aaron Scherzinger ; Cathrin Dierkes [Allemagne] ; Silvia Martin-Almedina [Royaume-Uni] ; Stefan Butz [Allemagne] ; Kristiana Gordon [Royaume-Uni] ; Michael Sch Fers [Allemagne] ; Klaus Hinrichs [Allemagne] ; Pia Ostergaard [Royaume-Uni] ; Dietmar Vestweber [Allemagne] ; Tobias Goerge [Allemagne] ; Sahar Mansour [Royaume-Uni] ; Xiaoyi Jiang ; Peter S. Mortimer [Royaume-Uni] ; Friedemann Kiefer [Allemagne]	VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations.
000034 (2017)	Marco Borri [Royaume-Uni] ; Kristiana D. Gordon [Royaume-Uni] ; Julie C. Hughes [Royaume-Uni] ; Erica D. Scurr [Royaume-Uni] ; Dow-Mu Koh [Royaume-Uni] ; Martin O. Leach [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Maria A. Schmidt [Royaume-Uni]	Magnetic Resonance Imaging–Based Assessment of Breast Cancer–Related Lymphoedema Tissue Composition
000117 (2016)	Magda M. Soares [Royaume-Uni] ; Georgia Keramida [Royaume-Uni] ; Daphne M. Glass [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Adrien Michael Peters [Royaume-Uni]	Lymph proteins may access peripheral blood without entering thoracic duct in patients with lymphatic dysfunction.
000145 (2016)	Viviana Cintolesi [Royaume-Uni] ; Anthony W B. Stanton [Royaume-Uni] ; Salena K. Bains [Royaume-Uni] ; Emma Cousins [Royaume-Uni] ; A Michael Peters [Royaume-Uni] ; Arnie D. Purushotham [Royaume-Uni] ; J Rodney Levick [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]	Constitutively Enhanced Lymphatic Pumping in the Upper Limbs of Women Who Later Develop Breast Cancer-Related Lymphedema.
000194 (2015)	Elisavet Fotiou [Royaume-Uni] ; Silvia Martin-Almedina [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Shin Lin [États-Unis] ; Kristiana Gordon [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Giles Atton [Royaume-Uni] ; Iona Jeffery [Royaume-Uni] ; David C. Rees [Royaume-Uni] ; Cyril Mignot [France] ; Julie Vogt [Royaume-Uni] ; Tessa Homfray [Royaume-Uni] ; Michael P. Snyder [États-Unis] ; Stanley G. Rockson [États-Unis] ; Steve Jeffery [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni]	Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
000301 (2014)	Peter S. Mortimer [Royaume-Uni] ; Stanley G. Rockson [États-Unis]	New developments in clinical aspects of lymphatic disease
000385 (2013)	Kristiana Gordon [Royaume-Uni] ; Dörte Schulte ; Glen Brice ; Michael A. Simpson ; M Guy Roukens ; Andreas Van Impel ; Fiona Connell ; Kamini Kalidas ; Steve Jeffery ; Peter S. Mortimer ; Sahar Mansour ; Stefan Schulte-Merker ; Pia Ostergaard	Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.
000387 (2013)	Gabriela E. Jones [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni] ; Anthony T. Moore [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Denise Williams [Royaume-Uni] ; Oliver Quarrell [Royaume-Uni] ; Angela F. Brady [Royaume-Uni] ; Isabel Spier [Allemagne] ; Filiz Hazan [Turquie] ; Oana Moldovan [Portugal] ; Dagmar Wieczorek [Allemagne] ; Barbara Mikat [Allemagne] ; Florence Petit [France] ; Christine Coubes [France] ; Robert A. Saul [États-Unis] ; Glen Brice [Royaume-Uni] ; Kristiana Gordon [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Pradeep C. Vasudevan [Royaume-Uni] ; Sahar Mansour [Royaume-Uni]	Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations
000456 (2013)	Amanda Saracino [Royaume-Uni] ; Kristiana Gordon [Royaume-Uni] ; Lorette Ffolkes [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]	Intralymphatic granulomas in lymphoedema secondary to anogenital granulomatosis
000465 (2013)	Kristiana Gordon [Royaume-Uni] ; Sarah L. Spiden [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sally Cottrell [Royaume-Uni] ; John Short [Royaume-Uni] ; Rohan Taylor [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Pia Ostergaard [Royaume-Uni]	FLT4/VEGFR3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update
000508 (2012)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Antonella Mendola [Belgique] ; Pradeep Vasudevan [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Andreas Van Impel [Pays-Bas] ; Anthony T. Moore [Royaume-Uni] ; Bart L. Loeys [Belgique] ; Arash Ghalamkarpour [Belgique] ; Alexandros Onoufriadis [Royaume-Uni] ; Ines Martinez-Corral ; Sophie Devery [Royaume-Uni] ; Jules G. Leroy [Belgique] ; Lut Van Laer [Belgique] ; Amihood Singer [Israël] ; Martin G. Bialer [États-Unis] ; Meriel Mcentagart [Royaume-Uni] ; Oliver Quarrell [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Richard C. Trembath [Royaume-Uni] ; Stefan Schulte-Merker [Pays-Bas] ; Taija Makinen ; Miikka Vikkula [Belgique] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]	Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
000511 (2012)	Katherine M. Burnand [Royaume-Uni] ; Daphne M. Glass ; Peter S. Mortimer ; Adrien Michael Peters	Lymphatic dysfunction in the apparently clinically normal contralateral limbs of patients with unilateral lower limb swelling.
000590 (2012)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Antonella Mendola [Belgique] ; Pradeep Vasudevan [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Andreas Van Impel [Pays-Bas] ; Anthony T. Moore [Royaume-Uni] ; Bart L. Loeys [Belgique] ; Arash Ghalamkarpour [Belgique] ; Alexandros Onoufriadis [Royaume-Uni] ; Ines Martinez-Corral [Royaume-Uni] ; Sophie Devery [Royaume-Uni] ; Jules G. Leroy [Belgique] ; Lut Van Laer [Belgique] ; Amihood Singer [Israël] ; Martin G. Bialer [États-Unis] ; Meriel Mcentagart [Royaume-Uni] ; Oliver Quarrell [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Richard C. Trembath [Royaume-Uni] ; Stefan Schulte-Merker [Pays-Bas] ; Taija Makinen [Royaume-Uni] ; Miikka Vikkula [Belgique] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]	Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
000614 (2011)	Katherine M. Burnand [Royaume-Uni] ; Daphne M. Glass ; Sumati Sundaraiya ; Peter S. Mortimer ; A Michael Peters	Popliteal node visualization during standard pedal lymphoscintigraphy for a swollen limb indicates impaired lymph drainage.
000620 (2011)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson ; Fiona C. Connell ; Colin G. Steward ; Glen Brice ; Wesley J. Woollard ; Dimitra Dafou ; Tatjana Kilo ; Sarah Smithson ; Peter Lunt ; Victoria A. Murday ; Shirley Hodgson ; Russell Keenan ; Daniela T. Pilz ; Ines Martinez-Corral ; Taija Makinen ; Peter S. Mortimer ; Steve Jeffery ; Richard C. Trembath ; Sahar Mansour	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
000621 (2011)	Russell H. Mellor [Royaume-Uni] ; Naomi Tate ; Anthony W B. Stanton ; Charlotte Hubert ; Taija M Kinen ; Alberto Smith ; Kevin G. Burnand ; Steve Jeffery ; J Rodney Levick ; Peter S. Mortimer	Mutations in FOXC2 in humans (lymphoedema distichiasis syndrome) cause lymphatic dysfunction on dependency.
000652 (2011)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Alexandros Onoufriadis [Royaume-Uni] ; Anne H. Child [Royaume-Uni] ; Jae Hwang [Royaume-Uni] ; Kamini Kalidas [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Richard Trembath [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]	Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype
000671 (2011)	John S. Ferguson [Royaume-Uni] ; Shymalar Gunatheesan [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Rob Hastings [Royaume-Uni] ; Ruth Newbury-Ecob [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Sahar Mansour [Royaume-Uni]	Primary lymphedema with coarctation of the aorta: Possible new syndrome or variant of Irons–Bianchi syndrome?
000698 (2011)	Katherine M. Burnand [Royaume-Uni] ; Daphne M. Glass [Royaume-Uni] ; Sumati Sundaraiya [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; A. Michael Peters [Royaume-Uni]	Popliteal Node Visualization During Standard Pedal Lymphoscintigraphy for a Swollen Limb Indicates Impaired Lymph Drainage
000700 (2011)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Colin G. Steward [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Wesley J. Woollard [Royaume-Uni] ; Dimitra Dafou [Royaume-Uni] ; Tatjana Kilo [Australie] ; Sarah Smithson [Royaume-Uni] ; Peter Lunt [Royaume-Uni] ; Victoria A. Murday [Royaume-Uni] ; Shirley Hodgson [Royaume-Uni] ; Russell Keenan [Royaume-Uni] ; Daniela T. Pilz [Royaume-Uni] ; Ines Martinez-Corral [Royaume-Uni] ; Taija Makinen [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Richard C. Trembath [Royaume-Uni] ; Sahar Mansour [Royaume-Uni]	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
000701 (2011)	Russell H. Mellor [Royaume-Uni] ; Naomi Tate [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Charlotte Hubert [Royaume-Uni] ; Taija M Kinen [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]	Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency

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List of associated KwdEn.i

Nombre de documents	Descripteur
32	Humans
27	Female
18	Male
17	Middle Aged
15	Aged
14	Adult
14	Lymphedema
14	Lymphedema (diagnostic imaging)
11	Lymphedema (etiology)
11	Lymphedema (genetics)
11	Lymphedema (physiopathology)
11	Mutation
8	Lymphoscintigraphy
7	Human
7	Radionuclide Imaging
6	Breast Neoplasms (complications)
6	Lymphedema (pathology)
6	Phenotype
5	Child
5	Lymphatic Vessels (diagnostic imaging)
5	Lymphatic system
4	Adolescent
4	Arm
4	Arm (diagnostic imaging)
4	Arm (pathology)
4	Breast Neoplasms (surgery)
4	Lymph Node Excision (adverse effects)
4	Lymphedema (congenital)
4	Pedigree
4	Technetium
3	Animals
3	Breast Neoplasms (diagnostic imaging)
3	Breast Neoplasms (physiopathology)
3	Breast cancer
3	Case-Control Studies
3	Foot
3	Immunoglobulins
3	Infant, Newborn
3	Injections, Subcutaneous
3	Lymph Nodes (diagnostic imaging)
3	Lymph node
3	Lymphatic
3	Lymphatic Metastasis
3	Lymphatic System (pathology)
3	Lymphatic System (physiopathology)
3	Lymphatic Vessels (pathology)
3	Lymphatic Vessels (physiopathology)
3	Radiopharmaceuticals (administration & dosage)
3	Scintigraphy
3	Treatment
3	Vascular Endothelial Growth Factor Receptor-3 (genetics)
3	Young Adult
2	Aged, 80 and over
2	Arm (blood supply)
2	Arm (physiopathology)
2	Autosomal character
2	Child, Preschool
2	Chronic Disease
2	Cohort Studies
2	Comparative study
2	Dominant character
2	Drainage
2	Dysfunction
2	Forearm
2	Forkhead Transcription Factors (genetics)
2	Genetic Predisposition to Disease
2	Genetic disease
2	Genetics
2	Hand
2	Heterozygote
2	Immunoglobulin G
2	Immunoglobulin G (administration & dosage)
2	Immunoglobulin G (blood)
2	Immunoglobulins (administration & dosage)
2	Indium Radioisotopes
2	Kinesin (genetics)
2	Leg (pathology)
2	Limb
2	Lipoedema
2	Lymph
2	Lymph Nodes (surgery)
2	Lymphedema (diagnosis)
2	Lymphedema (therapy)
2	Malignant tumor
2	Mammary gland
2	Microcephaly (genetics)
2	Organotechnetium Compounds (administration & dosage)
2	Quantitative analysis
2	Radiopharmaceuticals
2	Reproducibility of Results
2	Sensitivity and Specificity
2	Sequence Analysis, DNA
2	Subcutaneous Tissue (diagnostic imaging)
2	Syndrome
2	Technetium (administration & dosage)
2	Technetium Tc 99m Aggregated Albumin (administration & dosage)
2	Ultrasonography, Doppler, Color
2	Upper Extremity (diagnostic imaging)
1	Abnormalities, Multiple (genetics)
1	Acute myelogenous leukemia

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