last data update: 2011/10/14, 00:39

Website loading time

during the test: 0.14 s

cable connection (average): 0.5 s

DSL connection (average): 0.85 s

modem (average): 19.66 s

HTTP headers

Information about DNS servers

suggestadoctor.comA64.20.53.110IN14400
suggestadoctor.comMX0suggestadoctor.comIN14400
suggestadoctor.comSOAdns.trouble-free.netroot.dns.trouble-free.net200811025628800 7200 1209600 86400 IN 14400
suggestadoctor.comNSdns2.trouble-free.netIN14400
suggestadoctor.comNSdns.trouble-free.netIN14400

Received from the first DNS server

Request to the server "suggestadoctor.com"
You used the following DNS server:
DNS Name: dns2.trouble-free.net
DNS Server Address: 66.45.228.4#53
DNS server aliases:

HEADER opcode: REQUEST, status: NOERROR, id: 10586
flag: qr aa rd REQUEST: 1, ANSWER: 5, AUTHORITY: 0, ADDITIONAL: 3

REQUEST SECTION:
suggestadoctor.com. IN ANY

ANSWER SECTION:
suggestadoctor.com. 14400 IN SOA dns.trouble-free.net. root.dns.trouble-free.net. 2008110256 28800 7200 1209600 86400
suggestadoctor.com. 14400 IN NS dns.trouble-free.net.
suggestadoctor.com. 14400 IN NS dns2.trouble-free.net.
suggestadoctor.com. 14400 IN MX 0 suggestadoctor.com.
suggestadoctor.com. 14400 IN A 64.20.53.110

SECTION NOTES:
dns.trouble-free.net. 14400 IN A 66.45.228.79
dns2.trouble-free.net. 14400 IN A 66.45.228.4
suggestadoctor.com. 14400 IN A 64.20.53.110

Received 210 bytes from address 66.45.228.4#53 in 7 ms

Received from the second DNS server

Request to the server "suggestadoctor.com"
You used the following DNS server:
DNS Name: dns.trouble-free.net
DNS Server Address: 66.45.228.79#53
DNS server aliases:

HEADER opcode: REQUEST, status: NOERROR, id: 31871
flag: qr aa rd REQUEST: 1, ANSWER: 5, AUTHORITY: 0, ADDITIONAL: 3

REQUEST SECTION:
suggestadoctor.com. IN ANY

ANSWER SECTION:
suggestadoctor.com. 14400 IN SOA dns.trouble-free.net. root.dns.trouble-free.net. 2008110256 28800 7200 1209600 86400
suggestadoctor.com. 14400 IN NS dns2.trouble-free.net.
suggestadoctor.com. 14400 IN NS dns.trouble-free.net.
suggestadoctor.com. 14400 IN MX 0 suggestadoctor.com.
suggestadoctor.com. 14400 IN A 64.20.53.110

SECTION NOTES:
dns.trouble-free.net. 14400 IN A 66.45.228.79
dns2.trouble-free.net. 14400 IN A 66.45.228.4
suggestadoctor.com. 14400 IN A 64.20.53.110

Received 210 bytes from address 66.45.228.79#53 in 7 ms

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Location

IP: 64.20.53.110

continent: NA, country: United States (USA), city: Secaucus

Website value

rank in the traffic statistics: 899 317

There is not enough data to estimate website value.

Basic information

website build using CSS

code weight: 136.62 KB

text per all code ratio: 6 %

title: SuggestADoctor.com - Portal of Suggested and Recommended Doctors with Patient Reviews

description: the unique experience sharing portal about good Medical Doctors in USA

keywords: suggestion, doctor, MD, best

encoding: windows-1254

language: en

Website code analysis

one word phrases repeated minimum three times

two word phrases repeated minimum three times

three word phrases repeated minimum three times

B tags

List yourself

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Listed Doctors :

154,064

Patient Reviews & Recommendations:

10,825

939

Video Library

Cayce JEHAIMI MD

Fluorodeoxyglucose-Positron Emission Tomography (FDG-PET) is being more frequently used in the evaluation of patients with papillary thyroid carcinoma (PTC) who have serologic evidence of disease and a negative. radioiodine (RAI) scan. Imaging with FDG-PET may localize disease, and there is accruing evidence that, in adults, increased FDG uptake by metastatic lesions is associated with a poorer prognosis. The utility of FDG-PET in children with PTC has not been studied. In this limited retrospective study, FDG-PET does not appear to be a highly sensitive test for localizing tumor in children w... [more..] "Primary Pigmented Nodular Adrenocortical Disease İn A Patient With Carney Complex: A Case Report" [by Cayce JEHAIMI MD

Carney complex (CC) is a rare, familial, multiple endocrine neoplasia syndrome, characterized by cardiac myxomas, skin lentigenes, and endocrine tumors. The most common endocrine manifestation is PPNAD. A 14-year old girl was referred for further evaluation of Cushing syndrome (CS). The patient (pt) complained of hirsutism, weight gain, and acne. She had not reached menarche and had crossed growth percentiles from the 75th % 4 years prior, to

We describe a novel mutation of the SOX9 gene not associated with sex reversal.Skeletal anomalies at birth associated with any degree of genital ambiguity should warrant SOX9 gene analysis.Although our case report did not display sex reversal,the presence of hypospadias in association with abnormal long bone structures and Pierre-Robin sequence was enough evidence to suspect SOX9 gene defect. Campomelic Dysplasia (CD) is an autosomal dominant disorder typically characterized by bowing of the long bones,Pierre-Robin sequence,cleft palate and absent corpus collosum among others (1,2).The majorit... [more..] "Polycystic Ovaries And Adrenal Insufficiency İn A Young Pubescent Female With Lipoid Congenital Adrenal Hyperplasia Due To Splice Mutation Of The Star Gene: A Case Report & Review Of The Literature" [by Cayce JEHAIMI MD

U tags

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"Positron Emission Tomography İn The Management Of Papillary Thyroid Carcinoma İn Children: İs There A Role?" [by Cayce JEHAIMI MD]Fluorodeoxyglucose-Positron Emission Tomography (FDG-PET) is being more frequently used in the evaluation of patients with papillary thyroid carcinoma (PTC) who have serologic evidence of disease and a negative. radioiodine (RAI) scan. Imaging with FDG-PET may localize disease, and there is accruing evidence that, in adults, increased FDG uptake by metastatic lesions is associated with a poorer prognosis. The utility of FDG-PET in children with PTC has not been studied. In this limited retrospective study, FDG-PET does not appear to be a highly sensitive test for localizing tumor in children w... [more..]

"Primary Pigmented Nodular Adrenocortical Disease İn A Patient With Carney Complex: A Case Report" [by Cayce JEHAIMI MD]Carney complex (CC) is a rare, familial, multiple endocrine neoplasia syndrome, characterized by cardiac myxomas, skin lentigenes, and endocrine tumors. The most common endocrine manifestation is PPNAD. A 14-year old girl was referred for further evaluation of Cushing syndrome (CS). The patient (pt) complained of hirsutism, weight gain, and acne. She had not reached menarche and had crossed growth percentiles from the 75th % 4 years prior, to

"Novel Intervening Sequence Mutation At The 5 [by Cayce JEHAIMI MD]We describe a novel mutation of the SOX9 gene not associated with sex reversal.Skeletal anomalies at birth associated with any degree of genital ambiguity should warrant SOX9 gene analysis.Although our case report did not display sex reversal,the presence of hypospadias in association with abnormal long bone structures and Pierre-Robin sequence was enough evidence to suspect SOX9 gene defect. Campomelic Dysplasia (CD) is an autosomal dominant disorder typically characterized by bowing of the long bones,Pierre-Robin sequence,cleft palate and absent corpus collosum among others (1,2).The majorit... [more..]

"Polycystic Ovaries And Adrenal Insufficiency İn A Young Pubescent Female With Lipoid Congenital Adrenal Hyperplasia Due To Splice Mutation Of The Star Gene: A Case Report & Review Of The Literature" [by Cayce JEHAIMI MD]We report a case of Lipoid Congenital Adrenal Hyperplasia (LCAH) secondary to Steroidogenic Acute Regulatory (StAR) gene mutation in an adolescent female with bilateral ovarian cysts. StAR gene defects follow an autosomal recessive mode of inheritance and typically present with severe adrenal insufficiency during infancy. Both sexes can be affected equally. XY males often present with sex reversal, while XX females may develop gonadal failure later in life due to premature loss of ovarian follicles. Recently there have been reported cases of successful fertility outcomes in women with LCAH. In... [more..]

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04-19-2011

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Identification Of A Novel Compound Heterozygous Mutation Of The 5 Alpha-Reductase Type 2 (Srd5a2) Gene İn An Extreme Premature 46, Xy Male İnfant
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"Positron Emission Tomography İn The Management Of Papillary Thyroid Carcinoma İn Children: İs There A Role?"
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"Primary Pigmented Nodular Adrenocortical Disease İn A Patient With Carney Complex: A Case Report"
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"Novel Intervening Sequence Mutation At The 5
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"Polycystic Ovaries And Adrenal Insufficiency İn A Young Pubescent Female With Lipoid Congenital Adrenal Hyperplasia Due To Splice Mutation Of The Star Gene: A Case Report & Review Of The Literature"
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