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A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1

Annals of human genetics, 2015-03, Vol.79 (2), p.92-98

2015

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Effectiveness and Safety of Intense Pulsed Light in Hirsutism

Pakistan Journal of Medical and Health Sciences, 2022-01, Vol.16 (1), p.327-329

2022

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Melasma and its Association with Serum Iron Levels and Complete Blood Count

Pakistan Journal of Medical and Health Sciences, 2022-01, Vol.16 (1), p.352-354

2022

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Psychological Morbidity in patients with Idiopathic Hirsutism presenting for Laser Treatment at a Tertiary Care Hospital

Journal of Rawalpindi Medical College, 2021-09, Vol.25 (3), p.345-350

2021

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Facial lichen nitidus actinicus

Australasian journal of dermatology, 2012-05, Vol.53 (2), p.e16-e17

2012

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Langerhan cell histiocytosis: a child presenting with nine months history of fever

Journal of Ayub Medical College, Abbottabad, 2014-10, Vol.26 (4), p.633-635

2014

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Dermatological Clue to Diagnosis of Degos Disease in a 2-Year-Old With Obscure Chronic Abdominal Pain

Clinical pediatrics, 2008-03, Vol.47 (2), p.180-182

2008

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Constitutional and Behavioral Risk Factors for Chilblains: A Case-Control Study From Pakistan

Wilderness & environmental medicine, 2010-03, Vol.21 (1), p.17-21.e1

2010

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Drug induced linear IgA disease with unusual features: Koebner phenomenon, local insulin sensitivity and annular blister of the nipples

Acta dermatovenerologica Croatica, 2008, Vol.16 (4), p.215

2008

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Correlation between the severity and type of acne vulgaris lesions with serum vitamin D levels: A cases control study of HIT Hospital, Taxila

Journal of Pakistan Association of Dermatologists : JPAD, 2023-09, Vol.33 (3), p.906

2023

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Millipede Burn at an Unusual Site Mimicking Child Abuse in an 8-Year-Old Girl

Clinical pediatrics, 2008-06, Vol.47 (5), p.490-492

2008

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Why dermatology patients are hospitalized? A study from Pakistan

Acta dermatovenerologica Croatica, 2009, Vol.17 (2), p.113-117

2009

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Ross syndrome with generalized anhidrosis and localized disabling compensatory hyperhidrosis

Annals of Saudi medicine, 2008-01, Vol.28 (1), p.53-54

2008

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Hair Coil Strangulation—An Uncommon Cause of Penile Edema

Pediatric dermatology, 2007-07, Vol.24 (4), p.E33-E35

2007

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Diagnostic Value of Skin Manifestations in Neonates in First 72 Hours of Birth

Pakistan Journal of Medical and Health Sciences, 2022-01, Vol.16 (1), p.122-124

2022

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Rosai Dorfman disease-a rare entity report of two cases with nodal and extranodal involvement

Journal of the Pakistan Medical Association, 2008-06, Vol.58 (6), p.338-340

2008

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Model for Developing Research Culture Experience at HITEC Institute of Medical Sciences

Pakistan journal of public health, 2022-09, Vol.12 (2), p.106-111

2022

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GLY67ARG substitution in RSPO4 disrupts the WNT signaling pathway due to an abnormal binding pattern with LGRs leading to anonychia

RSC advances, 2017-01, Vol.7 (28), p.17357-17366

2017

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Depression in adult dermatology outpatients

Journal of the College of Physicians and Surgeons--Pakistan, 2010-12, Vol.20 (12), p.811-813

2010

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Colloid milium of the upper eyelid margins: A rare presentation

Ophthalmology (Rochester, Minn.), 2002-10, Vol.109 (10), p.1944-1946

2002

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Orf with unusual features

Journal of the College of Physicians and Surgeons--Pakistan, 2014-11, Vol.24 Suppl 3, p.S174-S175

2014

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Clinical characteristics of uremic pruritus in patients undergoing haemodialysis

Journal of the College of Physicians and Surgeons--Pakistan, 2006-02, Vol.16 (2), p.94

2006

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GLY67ARG substitution in RSPO4 disrupts the WNT signaling pathway due to an abnormal binding pattern with LGRs leading to anonychiaElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ra00762k

2017-03

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Late onset erythropoietic porphyria (Gunther's disease)

Journal of the College of Physicians and Surgeons--Pakistan, 2011-09, Vol.21 (9), p.564-566

2011

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Localized lesions in secondary syphilis

Journal of the College of Physicians and Surgeons--Pakistan, 2008-05, Vol.18 (5), p.303-304

2008

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A Novel Homozygous Nonsense Mutation in the PVRL4 Gene and Expansion of Clinical Spectrum of EDSS1

Effectiveness and Safety of Intense Pulsed Light in Hirsutism

Melasma and its Association with Serum Iron Levels and Complete Blood Count

Psychological Morbidity in patients with Idiopathic Hirsutism presenting for Laser Treatment at a Tertiary Care Hospital

Facial lichen nitidus actinicus

Langerhan cell histiocytosis: a child presenting with nine months history of fever

Dermatological Clue to Diagnosis of Degos Disease in a 2-Year-Old With Obscure Chronic Abdominal Pain

Constitutional and Behavioral Risk Factors for Chilblains: A Case-Control Study From Pakistan

Drug induced linear IgA disease with unusual features: Koebner phenomenon, local insulin sensitivity and annular blister of the nipples

Correlation between the severity and type of acne vulgaris lesions with serum vitamin D levels: A cases control study of HIT Hospital, Taxila

Millipede Burn at an Unusual Site Mimicking Child Abuse in an 8-Year-Old Girl

Why dermatology patients are hospitalized? A study from Pakistan

Ross syndrome with generalized anhidrosis and localized disabling compensatory hyperhidrosis

Hair Coil Strangulation—An Uncommon Cause of Penile Edema

Diagnostic Value of Skin Manifestations in Neonates in First 72 Hours of Birth

Rosai Dorfman disease-a rare entity report of two cases with nodal and extranodal involvement

Model for Developing Research Culture Experience at HITEC Institute of Medical Sciences

GLY67ARG substitution in RSPO4 disrupts the WNT signaling pathway due to an abnormal binding pattern with LGRs leading to anonychia

Depression in adult dermatology outpatients

Colloid milium of the upper eyelid margins: A rare presentation

Orf with unusual features

Clinical characteristics of uremic pruritus in patients undergoing haemodialysis

GLY67ARG substitution in RSPO4 disrupts the WNT signaling pathway due to an abnormal binding pattern with LGRs leading to anonychiaElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ra00762k

Late onset erythropoietic porphyria (Gunther's disease)

Localized lesions in secondary syphilis

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