A. Nanda

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Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

M. Simpson, J. R. McMillan, M. Akiyama, 2014, American journal of human genetics.

Genetic evidence for the involvement of NOTCH4 in rheumatoid arthritis and alopecia areata.

A. Nanda, S. Alfadhli, Arti Nanda, 2013, Immunology letters.

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

N. Rahman, P. Futreal, F. Muntoni, 2003, American journal of human genetics.

Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.

J. McGrath, J. Mellerio, Lu Liu, 2011, Acta dermato-venereologica.

Skin manifestations of COVID‐19 in children: Part 2

R. Grimalt, C. Bodemer, V. Kinsler, 2020, Clinical and experimental dermatology.

A novel mutation in the VDR gene in hereditary vitamin D‐resistant rickets

M. Akiyama, J. McGrath, V. Wessagowit, 2007, The British journal of dermatology.

Further characterization of ATP 6 V 0 A 2-related autosomal recessive cutis laxa

S. Mundlos, H. Kayserili, M. Kabra, 2012 .

Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

S. Mundlos, H. Kayserili, M. Kabra, 2012, Human Genetics.

Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children.

D. Kelsell, J. McGrath, C. Mein, 2010, The Journal of investigative dermatology.

Fetal Hydantoin Syndrome: A Case Report

A. Nanda, A. Kanwar, O. N. Bhakoo, 1989, Pediatric dermatology.

Susceptible and protective endothelial nitric oxide synthase gene polymorphism in alopecia areata in the Kuwaiti population

N. Kharrat, Ahmed Rebai, A. Nanda, 2008, Autoimmunity.

Alopecia in children.

A. Nanda, A. Al-Fouzan, 2000, Clinics in dermatology.

Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity

W. Al-Herz, K. Sullivan, R. Krüger, 2021, Frontiers in Immunology.

Cutaneous Lupus Erythematosus in Children: Experience from a Tertiary Care Pediatric Dermatology Clinic

H. Al-Ajmi, A. Nanda, H. Al-Enezi, 2016, Pediatric dermatology.

Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait.

L. Notarangelo, R. Geha, W. Al-Herz, 2012, Clinical immunology.

Skin manifestations of COVID‐19 in children: Part 1

R. Grimalt, C. Bodemer, V. Kinsler, 2020, Clinical and experimental dermatology.

How effective are intravenous immunoglobulins in pediatric dermatology

A. Nanda, 2009 .

Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait

J. McGrath, J. Mellerio, H. Al-Ajmi, 2018, International journal of dermatology.

A Survey of Childhood Psoriasis in Kuwait

A. Nanda, A. Al-Fouzan, 1994, Pediatric dermatology.

University of Dundee Mutations in GRHL 2 result in an autosomal-recessive ectodermal dysplasia syndrome

M. Simpson, J. R. McMillan, M. Akiyama, 2022 .

Mycosis fungoides in children and adolescents

H. Al-Ajmi, A. Nanda, 2013 .

Genetic analysis of interleukin-1 receptor antagonist and interleukin-1β single-nucleotide polymorphisms C−511T and C+3953T in alopecia areata: susceptibility and severity association

A. Nanda, S. Alfadhli, 2014, Clinical and Experimental Medicine.

Skin manifestations of COVID‐19 in children: Part 3

R. Grimalt, C. Bodemer, V. Kinsler, 2020, Clinical and experimental dermatology.

Clinicopathological features and HLA tissue typing in pemphigoid gestationis patients in Kuwait

A. Nanda, R. Dvořák, Q. Alsaleh, 2003, Clinical and experimental dermatology.

Thyroid Function, Autoantibodies, and HLA Tissue Typing in Children with Alopecia Areata

A. Nanda, Q. Alsaleh, I. Almuzairai, 2002, Pediatric dermatology.

Salient features and HLA markers of childhood psoriasis in Kuwait

A. Nanda, N. Al-sweih, A. Al-Fouzan, 2000, Clinical and experimental dermatology.

Phacomatosis pigmentovascularis: Report of four new cases

H. Al-Ajmi, A. Nanda, Y. Habeeb, 2016, Indian journal of dermatology, venereology and leprology.

UVB PHOTOTHERAPY IN CHILDHOOD PSORIASIS

A. Nanda, A. Al-Fouzan, 1995, Pediatric dermatology.

Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

S. Mundlos, H. Kayserili, M. Kabra, 2012, Human Genetics.

GAPO Syndrome: A Report of Two Siblings and a Review of Literature

A. Nanda, M. Al-Khawari, Q. Alsaleh, 2010, Pediatric dermatology.

Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3.

M. Simpson, J. McGrath, R. Betz, 2017, Journal of Investigative Dermatology.

Lipoid Proteinosis: Report of Four Siblings and Brief Review of the Literature

J. Anim, A. Nanda, Q. Alsaleh, 2001, Pediatric dermatology.

Chronic cutaneous graft‐versus‐host disease in children: A report of 14 patients from a tertiary care pediatric dermatology clinic

W. Al-Herz, A. Nanda, Mohammad Al-Otaibi, 2018, Pediatric dermatology.

Spectrum of autoimmune bullous diseases in Kuwait

A. Nanda, R. Dvořák, Q. Alsaleh, 2004, International journal of dermatology.

Linear IgA Bullous Disease of Childhood: An Experience from Kuwait

A. Nanda, R. Dvořák, Q. Alsaleh, 2006, Pediatric dermatology.

DERMATOPHYTOSIS OF CHILDREN IN KUWAIT: A PROSPECTIVE SURVEY

A. Nanda, K. Kubec, A. Al-Fouzan, 1993, International journal of dermatology.

Dermatophytosis of Children in Kuwait

A. Nanda, A. Al-Fouzan, 1992, Pediatric dermatology.

Congenital Linear Psoriasis: A Case Report

A. Nanda, A. Al-Fouzan, Hussein M. M. Hassab‐EI‐Naby, 1990, Pediatric dermatology.

Childhood Psoriasis: An Epidemiologic Survey of 112 Patients

Bhushan Kumar, A. Nanda, I. Kaur, 1990, Pediatric dermatology.

Bullous pemphigoid (BP) in an infant complicated by tuberculous meningoencephalitis

A. Nanda, R. Dvořák, Q. Alsaleh, 2007, International Journal of Dermatology.

KETOCONAZOLE IN THE TREATMENT OF CUTANEOUS LEISHMANIASIS IN KUWAIT

A. Nanda, R. Dvořák, Q. Alsaleh, 1995, International journal of dermatology.

Pemphigus in Kuwait

A. Nanda, R. Dvořák, Q. Alsaleh, 1999, International journal of dermatology.

Pityriasis (Tinea) Versicolor in Infancy

A. Nanda, O. N. Bhakoo, S. Kaur, 1988, Pediatric dermatology.

A Prospective Survey of Pediatric Dermatology Clinic Patients in Kuwait: An Analysis of 10,000 Cases

A. Nanda, Q. Alsaleh, F. Al‐Hasawi, 1999, Pediatric dermatology.

Clinicoepidemiological features and course of 43 cases of bullous pemphigoid in Kuwait

A. Nanda, R. Dvořák, Q. Alsaleh, 2006, Clinical and experimental dermatology.

Spectrum of autoimmune bullous diseases among children in Kuwait

Humoud Alsabah, A. Nanda, I. Almasry, 2020, Pediatric dermatology.

Skin Manifestations in Primary Immunodeficient Children

W. Al-Herz, A. Nanda, W. Al‐Herz, 2011, Pediatric dermatology.

A Prospective Survey of Skin Manifestations in Children With Inborn Errors of Immunity From a National Registry Over 17 Years

W. Al-Herz, A. Nanda, Mohammad Zainal, 2021, Frontiers in Immunology.

Alopecia Areata in Children: A Clinical Profile

A. Nanda, A. Al-Fouzan, F. Al‐Hasawi, 2002, Pediatric dermatology.

Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations.

R. Happle, M. Zenker, J. Fischer, 2022, European journal of medical genetics.

Semi-dominant GPNMB mutations in amyloidosis cutis dyschromica.

M. Simpson, J. Tolar, J. McGrath, 2019, The Journal of investigative dermatology.

Systematised naevus sebaceus resulting from post‐zygotic mutation in HRAS

J. McGrath, H. Al-Ajmi, M. Hide, 2017, The Australasian journal of dermatology.

FAMILIAL INFLAMMATORY LINEAR VERRUCOUS EPIDERMAL NEVUS (ILVEN)

A. Nanda, H. M. Hassab-El-Naby, Q. Alsaleh, 1994, International journal of dermatology.

Paraneoplastic pemphigus in association with B‐cell lymphocytic leukemia and hepatitis C: favorable response to intravenous immunoglobulins and prednisolone

A. Nanda, R. Dvořák, Q. Alsaleh, 2007, International journal of dermatology.

Noninfectious cutaneous granulomas in primary immunodeficiency disorders: report from a national registry.

W. Al-Herz, H. Al-Ajmi, A. Nanda, 2014, The American Journal of dermatopathology.

Pemphigus in pregnancy.

A. Nanda, S. Kaur, A. Kanwar, 1989, American journal of obstetrics and gynecology.

Childhood Lichen Planus: A Report of 23 Cases

H. Al-Ajmi, A. Nanda, Q. Alsaleh, 2001, Pediatric dermatology.

Neutrophilic Panniculitis in a child with MYSM1 deficiency

Arun Gupta, A. Adekile, A. Nanda, 2019, Pediatric dermatology.

‘Progressive erythematous papules and plaques in an infant: Sweet that is not so sweet!’: reply from authors

A. Nanda, A. Fekry, H. Al-Sabah, 2020, Clinical and experimental dermatology.

Association of linear IgA bullous disease of childhood with Crohn's disease

J. Anim, A. Nanda, R. Dvořák, 2004, International journal of dermatology.

Survey of Cutaneous Lesions in Indian Newborns

A. Nanda, O. N. Bhakoo, S. Kaur, 1989, Pediatric dermatology.

Congenital Yellow Nail Syndrome: A Case Report and Its Relationship to Nonimmune Fetal Hydrops

A. Nanda, Q. Alsaleh, FAHAD H. AL‐ESSA, 2010, Pediatric dermatology.

Type 2 segmental Hailey–Hailey disease with systematized bilateral arrangement

R. Happle, A. Nanda, H. Al-Sabah, 2014, International journal of dermatology.

Febrile ulceronecrotic Mucha-Habermann disease (pityriasis lichenoides et varioliformis acuta fulminans) associated with parvovirus infection.

A. Nanda, Mohammad Al-Otaibi, H. Al-Sabah, 2013, The American Journal of dermatopathology.

Temporal case clustering in pityriasis rosea: a regression analysis on 1379 patients in Minnesota, kuwait, and diyarbakir, Turkey.

N. Molinari, A. Nanda, A. Chuh, 2005, Archives of dermatology.

Drug-induced toxic epidermal necrolysis in developing countries.

A. Nanda, S. Kaur, 1990, Archives of dermatology.

Mycosis Fungoides in Arab Children and Adolescents: A Report of 36 Patients from Kuwait

M. Demierre, H. Al-Ajmi, A. Nanda, 2010, Pediatric dermatology.

Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23.

M. Simpson, S. Blumen, J. Tolar, 2017, American journal of human genetics.

Hair discoloration caused by etretinate.

A. Nanda, Q. Alsaleh, 1994, Dermatology.

Pigmentary Disorders and Vitiligo

A. Nanda, 2012 .

Cole disease due to a novel pathogenic variant in the ENPP1 gene

R. Betz, A. Nanda, A. AlLafi, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Consanguinity and Double Recessive Gene Pathology: Cutis Laxa (PYCR1) and Nephrotic Syndrome (PLCE1).

M. Simpson, J. McGrath, A. Onoufriadis, 2019, JAMA dermatology.

Rothmund‐Thomson Syndrome in Two Siblings

B. Radotra, A. Nanda, S. Kaur, 1989, Pediatric dermatology.

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population

O. Sarig, N. Shomron, R. Bergman, 2021, Experimental dermatology.

Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family

M. Simpson, J. R. McMillan, M. Akiyama, 2015, The British journal of dermatology.

Benign familial pemphigus (Hailey-Hailey disease) responsive to low dose cyclosporine.

A. Nanda, R. Dvořák, Q. Alsaleh, 2010, Indian journal of dermatology, venereology and leprology.

Mutations in PYCR1 cause cutis laxa with progeroid features

Peter Nürnberg, Stefan Mundlos, Barry Merriman, 2009, Nature Genetics.

FIXED DRUG ERUPTION AT THE SITE OF BCG VACCINATION

Rajeev Sharma, A. Nanda, A. Kanwar, 1988, Pediatric dermatology.

Congenital papulonodular eruption: presenting sign of congenital leukaemia cutis

A. Nanda, J. Madda, M. Al-Ajmi, 2012, Clinical and experimental dermatology.

Impact of next generation sequencing on diagnostics in a genetic skin disease clinic

M. Simpson, M. Akiyama, J. McGrath, 2013, Experimental dermatology.

Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).

M. Ramsay, T. Jenkins, J. McGrath, 2002, Human molecular genetics.

An Infant with Congenital Indurated Hairy Plaque

A. Nanda, M. Selim, H. Al-Sabah, 2011, Pediatric dermatology.

Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients

J. McGrath, D. Lipsker, S. Küry, 2019, The British journal of dermatology.

Multiple Milia in a Newborn with Congenital Malformations: Oral‐Facial‐Digital Syndrome Type 1

A. Nanda, Q. Alsaleh, A. Sharaf, 2010, Pediatric dermatology.

Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis

O. Sarig, E. Sprecher, A. Paller, 2020, Genetics in Medicine.

Syndromic inherited poikiloderma due to a de novo mutation in FAM111B

M. Simpson, M. Akiyama, J. McGrath, 2017, The British journal of dermatology.

Papules on the eyelids of an adolescent

A. Nanda, A. AlLafi, Z. Akbar, 2022, Pediatric dermatology.

Vascular Malformations and Neoplasms in Childhood

A. Nanda, 2012 .

Unilesional (Segmental) Mycosis Fungoides Presenting in Childhood

E. Calonje, A. Nanda, Q. Alsaleh, 2004, Pediatric dermatology.

Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas‐Papas and CHAND syndromes

P. Nürnberg, J. Altmüller, F. B. Basmanav, 2015, American journal of medical genetics. Part A.

Coexistence of pemphigus vulgaris with systemic lupus erythematosus

A. Nanda, R. Dvořák, Q. Alsaleh, 2004, International journal of dermatology.

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

M. Simpson, J. R. McMillan, M. Akiyama, 2015, The British journal of dermatology.

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis

O. Sarig, N. Shomron, J. McGrath, 2020, Experimental dermatology.

Novel TGM5 mutations in acral peeling skin syndrome

J. McGrath, E. Sprecher, M. Geel, 2015, Experimental dermatology.

Sweet's syndrome (acute febrile neutrophilic dermatosis) associated with adenocarcinoma of prostate and transitional cell carcinoma of urinary bladder

A. Nanda, Q. Alsaleh, K. Hussein, 2005, Journal of the European Academy of Dermatology and Venereology : JEADV.

Dorfman‐Chanarin Syndrome

Rajeev Sharma, A. Nanda, A. Kanwar, 1990, International journal of dermatology.

Clinicoepidemiological features of mycosis fungoides in Kuwait, 1991–2006

M. Demierre, H. Al-Ajmi, A. Nanda, 2010, International journal of dermatology.

Elucidation and management of 30 patients of drug induced toxic epidermal necrolysis (DTEN)

A. Nanda, S. Kaur, K. V. Sharma, 1990 .

Autoimmune Diseases Associated with Neurofibromatosis Type 1

A. Nanda, 2008, Pediatric dermatology.

Milia en plaque: a new site

A. Nanda, Q. Alsaleh, H. Al-Sabah, 2000, International journal of dermatology.

Autosomal Recessive Type II Cutis Laxa

J. Anim, S. Mallory, A. Nanda, 2004 .

Cardiomyopathy diagnosed in the eldest child harbouring p.S24X mutation in JUP

D. Kelsell, J. McGrath, A. South, 2016, The British journal of dermatology.

Linear hyperkeratotic spiny plaques in a child.

A. Nanda, A. Attia, Hamoud Al-Sabah, 2021, Pediatric dermatology.

Gerodermia Osteodysplastica/Wrinkly Skin Syndrome: Report of Three Patients and Brief Review of the Literature

A. Nanda, Q. Alsaleh, M. Nanda, 2008, Pediatric dermatology.

Extensive postzygotic mosaicism for a novel keratin 10 mutation in epidermolytic ichthyosis.

R. Happle, C. Has, J. Kohlhase, 2014, Acta dermato-venereologica.

Multidisciplinary care of epidermolysis bullosa during the COVID-19 pandemic—Consensus: Recommendations by an international panel of experts

C. Bodemer, J. Uitto, E. Sprecher, 2020, Journal of the American Academy of Dermatology.

Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse‐Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene

R. Grimalt, R. Betz, S. Pasternack, 2014, Pediatric dermatology.

Next generation diagnostics of heritable connective tissue disorders.

M. Simpson, M. Akiyama, J. McGrath, 2014, Matrix biology : journal of the International Society for Matrix Biology.

Keutel syndrome with overlapping features of cutis laxa: A new variant

J. Anim, A. Nanda, Q. Alsaleh, 2006, American journal of medical genetics. Part A.

Progressive erythematous papules and plaques in an infant

A. Nanda, A. Fekry, H. Al-Sabah, 2020, Clincal and Experimental Dermatology.

Incontinentia pigmenti in a father and daughter

H. Al-Ajmi, A. Nanda, Elham Rashidghamat, 2016, The British journal of dermatology.

What syndrome is this? Autosomal recessive type II cutis laxa.

J. Anim, A. Nanda, A. Al-Tawari, 2004, Pediatric dermatology.

Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

H. Al-Ajmi, A. Nanda, T. Takeichi, 2015, The British journal of dermatology.

CONCURRENT APPEARANCE OF ALOPECIA AREATA IN SIBLINGS

A. Nanda, Q. Alsaleh, F. Al‐Hasawi, 1995, Pediatric dermatology.