Celia Moss : rechercher sur Z-Library

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1

Dermatitis artefacta in children and adolescents

Journal:

Paediatrics and Child Health

Année:

2015

Langue:

english

Fichier:

PDF, 1.65 MB

english, 2015

2

HIV-1 vaccination by needle-free oral injection induces strong mucosal immunity and protects against SHIV challenge

Jones, Andrew T., Shen, Xiaoying, Walter, Korey L., LaBranche, Celia C., Wyatt, Linda S., Tomaras, Georgia D., Montefiori, David C., Moss, Bernard, Barouch, Dan H., Clements, John D., Kozlowski, Pamel

Journal:

Nature Communications

Année:

2019

Langue:

english

Fichier:

PDF, 1.97 MB

english, 2019

3

EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype–phenotype correlation?

Kenneth Maclean, Stephen A. Holme, Elizabeth Gilmour, Mark Taylor, Heide Scheffer, Nicole Graf, Grahame H.H. Smith, Ella Onikul, Hans van Bokhoven, Celia Moss, Lesley C. Adès

Journal:

American Journal of Medical Genetics Part A

Année:

2007

Langue:

english

Fichier:

PDF, 191 KB

english, 2007

4

Misunderstandings: a qualitative study of primary care consultations in multilingual settings, and educational implications

Celia Roberts, Becky Moss, Val Wass, Srikant Sarangi, Roger Jones

Journal:

Medical Education

Année:

2005

Langue:

english

Fichier:

PDF, 127 KB

english, 2005

5

Allergy to non-toxoid constituents of vaccines and implications for patch testing

Neil H. Cox, Celia Moss, Angela Forsyth

Journal:

Contact Dermatitis

Année:

1988

Fichier:

PDF, 469 KB

1988

6

Does SNAI2 mutation cause human piebaldism and Waardenburg syndrome?

Mirhadi, Sara, Spritz, Richard A., Moss, Celia

Journal:

American Journal of Medical Genetics Part A

Année:

2020

Fichier:

PDF, 344 KB

2020

7

Cytogenetic and molecular evidence for cutaneous mosaicism: The ectodermal origin of Blaschko lines

Journal:

American Journal of Medical Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 46 KB

english, 1999

8

Osteogenic sarcoma in the Rothmund-Thomson syndrome

Leonard, Andrea, Craft, Alan W., Moss, Celia, Malcolm, Archie J.

Journal:

Medical and Pediatric Oncology

Année:

1996

Langue:

english

Fichier:

PDF, 377 KB

english, 1996

9

Deletion of the SLUG (SNAI2) gene results in human piebaldism

Manuel Sánchez-Martín, Jesús Pérez-Losada, Arancha Rodríguez-García, Belén González-Sánchez, Bruce R. Korf, W. Kuster, Celia Moss, Richard A. Spritz, I. Sánchez-García

Journal:

American Journal of Medical Genetics Part A

Année:

2003

Langue:

english

Fichier:

PDF, 316 KB

english, 2003

10

Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis

Jan Hellemans, Philippe Debeer, Michael Wright, Andreas Janecke, Klaus W. Kjaer, Peter C.M. Verdonk, Ravi Savarirayan, Lina Basel, Celia Moss, Johannes Roth, Albert David, Anne De Paepe, Paul Coucke,

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 173 KB

english, 2006

11

End-stage renal failure in adolescence with Sjögren’s syndrome autoantibodies SSA and SSB

Sally Johnson, Sally-Anne Hulton, Marie-Anne Brundler, Celia Moss, Aarnoud Huissoon, C. Mark Taylor

Journal:

Pediatric Nephrology

Année:

2007

Langue:

english

Fichier:

PDF, 279 KB

english, 2007

12

Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex.

Smith, Frances J. D., Corden, Laura D., Rugg, Elizabeth L., Ratnavel, Ravi, Leigh, Irene M., Moss, Celia, Tidman, Michael J., Hohl, Daniel, Huber, Marcel, Kunkeler, Lia, Munro, Colin S., Lane, E. Birg

Journal:

The Journal of Investigative Dermatology

Année:

1997

Fichier:

PDF, 1.16 MB

1997

13

A Recurrent Homozygous Nonsense Mutation within the LAMA3 Gene as a Cause of Herlitz Junctional Epidermolysis Bullosa in Patients of Pakistani Ancestry: Evidence for a Founder Effect.

McGrath, John A., Kivirikko, Sirpa, Ciatti, Sabatino, Moss, Celia, Christiano, Angela M., Uitto, Jouni

Journal:

The Journal of Investigative Dermatology

Année:

1996

Fichier:

PDF, 1.21 MB

1996

14

A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis

Moss, Celia, Martinez-Mir, Amalia, Lam, HaMut, Tadin-Strapps, Marija, Kljuic, Ana, Christiano, Angela M.

Journal:

The Journal of Investigative Dermatology

Année:

2004

Langue:

english

Fichier:

PDF, 1.30 MB

english, 2004

15

Gonosomal Mosaicism for a Nonsense Mutation (R1947X) in the NF1 Gene in Segmental Neurofibromatosis Type 1

Consoli, Claudia, Moss, Celia, Green, Stuart, Balderson, Debra, Cooper, David N, Upadhyaya, Meena

Journal:

The Journal of Investigative Dermatology

Année:

2005

Langue:

english

Fichier:

PDF, 237 KB

english, 2005

16

Impaired contact hypersensitivity in untreated psoriasis and the effects of photochemotherapy and dithranol/UV-B

CELIA MOSS, P.S. FRIEDMANN, SAM SHUSTER

Journal:

British Journal of Dermatology

Année:

1981

Langue:

english

Fichier:

PDF, 341 KB

english, 1981

17

Serum 25-OH vitamin D after photochemotherapy

SAM SHUSTER, LAWRENCE CHADWICK, CELIA MOSS, JANET MARKS

Journal:

British Journal of Dermatology

Année:

1981

Langue:

english

Fichier:

PDF, 467 KB

english, 1981

18

How does PUVA inhibit delayed cutaneous hypersensitivity?

CELIA MOSS, P.S. FRIEDMANN, SAM SHUSTER

Journal:

British Journal of Dermatology

Année:

1982

Langue:

english

Fichier:

PDF, 1.74 MB

english, 1982

19

The effect of altering area of application and dose per unit area on sensitization by DNCB

S. I. WHITE, P. S. FRIEDMANN, CELIA MOSS, JUDY M. SIMPSON

Journal:

British Journal of Dermatology

Année:

1986

Langue:

english

Fichier:

PDF, 1.60 MB

english, 1986

20

Anhidrotic and achromians lesions in incontinentia pigmenti

CELIA MOSS, P. INCE

Journal:

British Journal of Dermatology

Année:

1987

Langue:

english

Fichier:

PDF, 3.17 MB

english, 1987

21

A sweating abnormality in incontinentia pigmenti

Celia Moss, P. Ince

Journal:

British Journal of Dermatology

Année:

1987

Langue:

english

Fichier:

PDF, 44 KB

english, 1987

22

Genetic control of sebum excretion and acne—a twin study

Journal:

British Journal of Dermatology

Année:

1989

Langue:

english

Fichier:

PDF, 149 KB

english, 1989

23

Rothmund-Thomson syndrome: a report of two patients and a review of the literature

Journal:

British Journal of Dermatology

Année:

1990

Langue:

english

Fichier:

PDF, 2.02 MB

english, 1990

24

Dermatology and the human gene map

Journal:

British Journal of Dermatology

Année:

1991

Langue:

english

Fichier:

PDF, 538 KB

english, 1991

25

Precocious puberty in a boy with a widespread linear epidermal naevus

CELIA MOSS, J.M. PARKIN, J.S. COMAISH

Journal:

British Journal of Dermatology

Année:

1991

Langue:

english

Fichier:

PDF, 2.17 MB

english, 1991

26

Atlas of Genodermatoses

Journal:

British Journal of Dermatology

Année:

2006

Langue:

english

Fichier:

PDF, 432 KB

english, 2006

27

Degos disease: a new simulator of non-accidental injury

CELIA MOSS, EVANGELINE WASSMER, GEOFF DEBELLE, SCOTT HACKETT, HELEN GOODYEAR, ROGER MALCOMSON, CLIVE RYDER, SPYROS SGOUROS, HOSSAIN SHAHIDULLAH

Journal:

Developmental Medicine & Child Neurology

Année:

2009

Langue:

english

Fichier:

PDF, 332 KB

english, 2009

28

Links Between Granuloma Annulare, Necrobiosis Lipoidica Diabeticorum and Childhood Diabetes: A Matter of Time?

James E. Davison, Alison Davies, Celia Moss, Jeremy M. W. Kirk, Saleem M. Taibjee, J. Chizo Agwu

Journal:

Pediatric Dermatology

Année:

2010

Langue:

english

Fichier:

PDF, 210 KB

english, 2010

29

Diarrhea Associated with Propranolol Treatment for Hemangioma of Infancy (HOI)

JOSEPH ABBOTT, MANOJ PARULEKAR, HOSSAIN SHAHIDULLAH, SALEEM TAIBJEE, CELIA MOSS

Journal:

Pediatric Dermatology

Année:

2010

Langue:

english

Fichier:

PDF, 55 KB

english, 2010

30

Dilated Cardiomyopathy In Epidermolysis Bullosa: A Retrospective, Multicenter Study—Response

SALEEM M. TAIBJEE, CELIA MOSS

Journal:

Pediatric Dermatology

Année:

2010

Langue:

english

Fichier:

PDF, 51 KB

english, 2010

31

Compound allergy to a skin marker for patch testing: a chromatographic analysis

Neil H. Cox, Celia Moss, Michael F. Hannon

Journal:

Contact Dermatitis

Année:

1989

Fichier:

PDF, 427 KB

1989

32

A New Way to Classify Genetic Skin Disease

Journal:

The Journal of Investigative Dermatology

Année:

2009

Langue:

english

Fichier:

PDF, 71 KB

english, 2009

33

The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia

Unsworth, Harriet C, Teh, Muy-Teck, Rüschendorf, Franz, Sinclair, Claire, Hopsu-Havu, Väinö K, Tidman, Nicholas, Moss, Celia, Blaydon, Diana C, Ishii, Yoshiyuki, O'Toole, Edel A

Journal:

Nature Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 420 KB

english, 2006

34

A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene

Antti M. Salo, Helen Cox, Peter Farndon, Celia Moss, Helen Grindulis, Maija Risteli, Simon P. Robins, Raili Myllylä

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 944 KB

english, 2008

35

Genetic counselling in hypomelanosis of Ito: case report and review

Celia Moss, John Burn

Journal:

Clinical Genetics

Année:

1988

Langue:

english

Fichier:

PDF, 647 KB

english, 1988

36

Letter to the Editors : Isolated radial ray defect may be due to Rothmund-Thomson syndrome

Celia Moss, C. J. Bacon, R. F. Mueller

Journal:

Clinical Genetics

Année:

1990

Langue:

english

Fichier:

PDF, 173 KB

english, 1990

37

A Homozygous Nonsense Mutation in the α3 Chain Gene of Laminin 5 (LAMA3) in Herlitz Junctional Epidermolysis Bullosa: Prenatal Exclusion in a Fetus at Risk

John A. McGrath, Sirpa Kivirikko, Sabatino Ciatti, Celia Moss, M.Giles S. Dunnill, Robin A.J. Eady, Charles H. Rodeck, Angela M. Christiano, Jouni Uitto

Journal:

Année:

1995

Fichier:

PDF, 214 KB

1995

38

Interpretation of changes in the activity of creatine kinase MB isoenzyme in serum after coronary artery bypass grafting

S.Y. Farah, D.W. Moss, P. Ribeiro, Celia M. Oakley, R.N. Sapsford

Journal:

Clinica Chimica Acta

Année:

1984

Langue:

english

Fichier:

PDF, 488 KB

english, 1984

39

Evolving lesions of phakomatosis pigmentokeratotica

Salim Asad, Celia Moss

Journal:

Journal of the American Academy of Dermatology

Année:

2004

Langue:

english

Fichier:

PDF, 43 KB

english, 2004

40

Tuberculous abscess in a 2-year-old resembling clinically and radiologically a lymphatic malformation

Simone Laube, Jane Clarke, Dakshish Parikh, Celia Moss

Journal:

Journal of the American Academy of Dermatology

Année:

2004

Langue:

english

Fichier:

PDF, 43 KB

english, 2004

41

Two families with Greither's syndrome caused by a keratin 1 mutation

Joanna E. Gach, Colin S. Munro, E. Birgitte Lane, Neil J. Wilson, Celia Moss

Journal:

Journal of the American Academy of Dermatology

Année:

2005

Langue:

english

Fichier:

PDF, 159 KB

english, 2005

42

Macrocephaly–cutis marmorata telangiectatica congenita: A case report and review of salient features

Ruwani Katugampola, Celia Moss, Caroline Mills

Journal:

Journal of the American Academy of Dermatology

Année:

2008

Langue:

english

Fichier:

PDF, 344 KB

english, 2008

43

Randomised controlled study of early pulsed dye laser treatment of uncomplicated childhood haemangiomas: results of a 1-year analysis

Kapila Batta, Helen M Goodyear, Celia Moss, Hywel C Williams, Louise Hiller, Ruth Waters

Journal:

Année:

2002

Langue:

english

Fichier:

PDF, 1.29 MB

english, 2002

44

Early pulsed-dye laser treatment of childhood haemangiomas

Kapila Batta, Celia Moss, Ruth Waters, Hywel C Williams, Louise Hiller

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 48 KB

english, 2003

45

Hereditary bullous disorders

Journal:

Current Paediatrics

Année:

1995

Langue:

english

Fichier:

PDF, 7.27 MB

english, 1995

46

Genetic skin disorders

Journal:

Seminars in Neonatology

Année:

2000

Langue:

english

Fichier:

PDF, 155 KB

english, 2000

47

A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma (NEMO)

Jonathan Zonana, Melissa E. Elder, Lynda C. Schneider, Seth J. Orlow, Celia Moss, Mahin Golabi, Stuart K. Shapira, Peter A. Farndon, Diane W. Wara, Stephanie A. Emmal, Betsy M. Ferguson

Journal:

The American Journal of Human Genetics

Année:

2000

Langue:

english

Fichier:

PDF, 441 KB

english, 2000

48

Muscular dystrophy with large mitochondria associated with mutations in the CHKB gene in three British patients: Extending the clinical and pathological phenotype

Quinlivan, Ros, Mitsuahashi, Satomi, Sewry, Caroline, Cirak, Sebahattin, Aoyama, Chieko, Mooore, David, Abbs, Stephen, Robb, Stephanie, Newton, Tina, Moss, Celia, Birchall, Daniel, Sugimoto, Hiroyuki,

Journal:

Neuromuscular Disorders

Année:

2013

Langue:

english

Fichier:

PDF, 1.44 MB

english, 2013

49

CUTANEOUS REACTIONS TO ALUMINIUM IN VACCINES: AN AVOIDABLE PROBLEM

Cox, N.H, Moss, Celia, Forsyth, Angela

Journal:

Année:

1988

Langue:

english

Fichier:

PDF, 177 KB

english, 1988

50

Duplicate reporting of patients with Rothmund-Thomson syndrome

Journal:

Journal of the American Academy of Dermatology

Année:

1989

Langue:

english

Fichier:

PDF, 434 KB

english, 1989